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Jean George joined Advanced Technology Ventures
as a Partner in 2002, with 20 years of experience in the biopharmaceutical
industry, including 10 years at Genzyme Corporation. Jean assesses
new deals in the life sciences and therapeutics markets, and utlizes
her operational skills to actively assist portfolio companies on
their strategic planning and development. Jean is currently on the
Boards of NuGenesis Technologies Corp. and Microbia, Inc.
Prior to joining ATV, Jean was a Director at BancBoston
Ventures, where she led the health care team’s investment
activity in NuGenesis Technologies Corp., Microbia, Inc., Syntonix
Pharmaceuticals and Neurometrix, Inc. Previously, during Jean’s
tenure at Genzyme, she held a variety of operational roles in marketing,
product development and business development, including Vice President
of Global Sales and Marketing. Jean was a member of the founding
team of the Genzyme Tissue Repair Division, and held responsibilities
for identifying new product opportunities and potential acquisition
candidates for the Therapeutic Products Division. In addition to
her extensive operating background, Jean spent six years working
in chemistry and bioresearch fields.
Jean earned an MBA from Simmons College Graduate
School of Management and a BS in Biology from the University of
Maine.
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Mr. Mills has over 21 years of venture capital experience,
and focuses on investments in the biotechnology, emerging pharmaceutical
and medical technology sectors. He is currently a Director of Ardais
Corporation (Lead Director), Enanta Pharmaceuticals Inc. and Stereotaxis,
Inc., and is a member of the Research and Technology Development
Committee and Equity Subcommittee of Beth Israel Deaconess Medical
Center (Harvard).
Before joining Advent, Mr. Mills spent eleven years
with The Venture Capital Fund of New England as a General Partner.
His specific area of responsibility was the partnership's pharmaceutical,
biotechnology and medical device portfolio. Prior to that, he spent
seven years at PaineWebber Ventures/Ampersand Ventures in Boston,
where as a Managing General Partner he concentrated on early stage
technology and biotechnology investments for a series of partnerships
affiliated with PaineWebber.
Mr. Mills received an A.B. in Chemistry, cum laude,
from Princeton University, an S.M. in Chemistry from the Massachusetts
Institute of Technology (organometallic photochemistry) and an M.S.
in Management from MIT's Sloan School of Management.
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Matt Hermann actively leads Ascension Health Ventures’
efforts to identify and fund innovative companies that can directly
benefit Ascension Health’s ministries and offer the potential
for strong investment returns. Before joining Ascension Health Ventures,
he served for five years, most recently as vice president with Atlantic
Medical Management, LLC, a New York-based venture capital management
company focused on early- to mid-stage healthcare services and information
technology companies. Prior to that, Mr. Hermann served in financial
management roles at two publicly traded healthcare companies, Nutrition
21, Inc. and Regeneron Pharmaceuticals, Inc., and worked at J.P.
Morgan Chase & Co. and PricewaterhouseCoopers in New York City.
Mr. Hermann is a board observer at several portfolio
companies. He holds a Bachelor’s of Science degree in engineering
science from Tufts University, College of Engineering, and a master’s
of business administration degree in finance from New York University,
Leonard N. Stern Graduate School of Business.
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Dr. Maggie Flanagan is the Global Alliance Director
for Enabling Science, Technology and Information at AstraZeneca
Pharmaceuticals. Prior to joining AstraZeneca, Dr. Flanagan was
the Senior Director, Business Development at Hybridon, Inc., Cambridge,
MA, President, BioAlliance, Inc., Lexington, MA, Director, Licensing
and Proprietary Drug Discovery, Oncogene Science Inc., Cambridge,
MA, and Senior Scientist, (Marion) Merrell Dow Pharmaceuticals,
Cincinnati, OH. She has a B.S. in Chemistry from the University
of Kansas, and a Ph.D. in Physical Chemistry from Indiana University,
Bloomington.
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Jim Fickett entered the field of bioinformatics
in 1980 as one of the founders of GenBank. He was active in the
development of sequence analysis algorithms for many years, pioneering
in the development of algorithms for gene structure prediction and
analysis of transcriptional regulatory regions. He joined SmithKline
Beecham in 1996 and headed the Bioinformatics Research Group there.
He now heads scientific and strategic aspects of IS and Informatics
for AstraZeneca.
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Jean-François Formela joined Atlas Venture
in 1993. Previously, he was Senior Director, Medical Marketing and
Scientific Affairs at Schering-Plough in the US. During his tenure
there, he was responsible for the marketing of Intron A, Schering-Plough's
alpha-interferon. In his last position at Schering-Plough, he directed
the US Phase IV studies in all therapeutic areas, as well as the
health economics, medical information, and biotechnology pre-marketing
groups. As a medical doctor, Jean-François practiced emergency
medicine at Necker University hospital in Paris.
Since joining Atlas Venture, Jean-François
has been involved in the formation of companies such as ArQule (Nasdaq:
ARQL), MorphoSys (Neuer Markt: MORG), Exelixis (Nasdaq: EXEL), deCODE
genetics (Nasdaq: DCGN), Variagenics (Nasdaq: VGNX), Structural
GenomiX, CellZome, Archemix and Akceli.
Jean-François received his MD from Paris University School
of Medicine, and his MBA from Columbia University.
Board participation includes:
Achillion Pharmaceuticals, Inc, Akceli, Inc, Cellzome AG, Compound
Therapeutics, deCODE genetics, Inc, Exelixis, Inc, Nuvelo, Inc.,
NxStage Medical, Structural GenomiX, Inc
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Michael King is a Managing Director and Senior Equity
Research Analyst in the Health Care Group at Banc of America Securities
LLC where he covers the biotechnology sector.
Mike joined Banc of America Securities in 2002 from
Robertson Stephens, where he had been a Managing Director and Senior
Biotechnology Analyst since 1998. Prior to that, he served as senior
biotechnology analyst at Vector Securities from 1996 to 1998 and
at Dillon, Read & Co. from 1994 to 1996. He has also held positions
at D. Blech & Company, Alex Brown and Sons, Hambrecht &
Quist and Kidder, Peabody & Company. He earned a BBA with honors
in finance from Baruch College.
Mike was ranked fourth for his stock-picking accuracy
in The Wall Street Journal’s annual “Best on the Street”
survey in 2001 and was given the Institutional Investor Home-Run
Hitter award in 2000 for his coverage of OSI Pharmaceuticals.
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Dr. Ober is the Senior Managing Executive with overall
responsibility for the company. Dr. Ober comes to Beyond Genomics
from Synergy Health Care, Inc., a company that he founded and where
he served as President and CEO from 1995 to 2000. Dr. Ober was instrumental
in establishing Synergy as a leading informatics company in the
Health Care and Pharmaceutical Industries. Synergy is now a division
of Quintiles Transnational, the largest provider of outsourced drug
development, commercialization and health care informatics to the
global pharmaceutical industry. In addition to over 15 years in
the health care, informatics and life sciences, Dr. Ober received
his MBA from Harvard Business School and his MD degree from Boston
University School of Medicine.
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Dr. Shahi is a physician with training in molecular
biochemistry and in international health policy and management.
He is a leading expert on change management and strategic program
implementation in healthcare and the life sciences. He has played
a key role in the development of several major international initiatives
including the International Vaccine Institute (now based in Seoul,
Korea) and the Asia-Pacific International Molecular Biology Network,
and has served as advisor and consultant to leading international
organizations, governments, corporations and foundations. He has
also been actively involved in establishing and providing strategic
and management input to a range of start-up enterprises including
Lynk Biotechnologies, Asia Pacific Genomics, and DNA Phenomics,
and in helping a growing number of US, European and Australian enterprises
build their operations in Asia.
Dr. Shahi has authored over 50 articles, refereed journal papers
and conference presentations, and served as lead editor for International
Perspectives on Environment, Development and Health: Toward a Sustainable
World (GS Shahi, BS Levy, A Binger, T Kjellstrom and RS Lawrence,
Springer Publishing Company, New York, 1997). He is currently putting
the final touches to his latest book, BioBusiness in Asia: How Asian
Countries Can Capitalize on the Life Science Revolution. In addition,
among other activities, he currently teaches Technology and World
Change at the Singapore Management University.
[MBBS, PhD - National University of Singapore;
MPH - Harvard University; Warren Weaver Fellow - The Rockefeller
Foundation]
BioEnterprise Asia; email: gurinder.shahi@bioenterprise.org
web: http://www.bioenterprise.org;
tel: +65-9423-9133 (international roaming)
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During the course of her career, Ms. Abou-Jamra
has established a solid network of contacts in U.S. Biotechnology
and venture capital firms.
Before founding BioExec Ventures, LLC, Ms. Abou-Jamra
was in business development at Acumen Sciences, a newly-launched
research firm for the biotechnology and pharma industries. Previous
to Acumen, she held a business development position at Incyte Genomics.
Before joining Incyte she was involved in the early stage of Pure
Tech Ventures, which creates and develops companies based on innovative
life science technologies that often represent the convergence of
several areas of research and development. Ms. Abou-Jamra now serves
as a business advisor for that group.
Her past bio/pharma experience includes a successful
sales, Marketing and Business Development position at Boiron Laboratories
and Bayer Corporation. Prior to that she lead NPC Inc., a private
consulting firm specializing in business, marketing, and fundraising
for customers such as Alliance Imaging Inc., and ATI systems.
In addition to her career pursuits, Ms. Abou-Jamra
has also served on several finance and fundraising committees, including
Senator John Kerry's campaign finance committee and service as a
board member for the Massachusetts Women's Political Caucus, where
she chaired the Abigail Adams fundraising event for two years. She
is also a member of the Academy of Managed Care Pharmacists, American
Pharmaceutical Association, the Boston Association of Retail Druggists
and Fenway Community Health Center.
Ms. Abou-Jamra graduated from the Bouve College
of Health Sciences, Northeastern University with a degree in Pharmacy.
She is fluent in French, English, and Arabic..
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Dr. Vibha Ahuja did her M.Sc. and PhD. In Microbiology
from Department of Microbiology, Panjab University, Chandigarh,
India. She had been working in BCIL for last 10 years and has undertaken
several assignments in the area of technology transfer, consultancy
ranging from conducting techno market surveys, preparation of project
feasibility reports, to preparation of business plans and status
studies and organizing workshops on current topics of interest in
biotechnology like biosafety regulations, biodiversity conservation
etc. She is also associated with the preparation of the National
Biodiversity Strategy and Action Plan (NBSAP) project of UNDP/GEF
being coordinated by BCIL on behalf of Ministry of Environment and
Forests, Government of India.
She has been associated with the recent market assessment of various
biotech sectors in India and has participated actively in the preparation
of a document for UNIDO on Perspective of Biotechnology in the Asia
Pacific Region. She has presnted India's biotechnology scene in
international conferences at Singapore and Trieste (Italy), organized
by agencies such as Frost & Sullivan and the International Centre
for Genetic Engineering and Biotechnology.
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Rob focuses on investment opportunities in life
sciences. Rob was previously a Program Executive with Vertex Pharmaceuticals,
where he led cancer drug development strategy and oversaw pre-clinical/clinical
development, marketing, regulatory, and business activities. He
was also a member of the Joint Research Committee for the $800 million
Vertex-Novartis collaboration. Prior to that, Rob was an Associate
with McKinsey & Company where he served clients in the pharmaceutical,
medical device, insurance, and healthcare payer-provider industries.
He was previously a Researcher and Attending Physician at Dana-Farber
Cancer Institute, Brigham & Women’s Hospital, and Harvard
Medical School. Rob is a diplomate in both internal medicine and
oncology. Rob is a Director or Board participant of EpiGenesis Pharmaceuticals,
Novalar Pharmaceuticals and GlycoFi. Rob is a Phi Beta Kappa graduate
of Johns Hopkins University and received his M.D. from Johns Hopkins
University School of Medicine.
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G. Steven Burrill has been involved in the growth
and prosperity of the biotechnology industry for 35 years. An early
pioneer, Mr. Burrill is one of the original architects of the industry
and one of its most avid and sustained developers. Mr. Burrill currently
serves as Board Chairman for Paradigm Genetics (NASDAQ: PDGM) and
Pyxis Genomics and as a Board member of Catalyst Biosciences, DepoMed
(AMEX: DMI), Galapagos Genomics, Inhibitex (observer), Targacept,
and Third Wave Technologies (NASDAQ: TWTI). Prior to founding Burrill
& Company in 1994, he spent 28 years with Ernst & Young,
directing and coordinating the firm's services to clients in the
biotechnology/life sciences/high technology/manufacturing industries
worldwide. In 2002, Mr. Burrill was recognized as the biotech investment
visionary by the prestigious Scientific American magazine (The Scientific
American 50). Mr. Burrill is a founder of the Foundation for the
National Medals of Science and Technology. He also serves on the
Boards of the Bay Area Bioscience Center, the Bay Area Science Infrastructure
Consortium, the California Healthcare Institute, the Exploratorium,
and the Kellogg Center for Biotechnology. Mr. Burrill is also on
the Advisory Boards of the University of California, San Francisco
(UCSF) Foundation, the University of Hawaii Medical School, and
the University of Wisconsin Foundation. In addition, he is a member
of The World Bank’s “Out of the Box” group as
well as an adjunct professor at UCSF.
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Pierre Cantin joined CDP Capital – Technology
Ventures in 2001 and currently holds the position of Senior Partner.
Mr. Cantin has nearly 20 years of experience, with 10 years in the
life sciences sector, specifically mergers and acquisitions. Before
joining CDP Capital – Technology Ventures, he held the position
of Senior Vice-President and Director of KPMG Corporate Finance,
where he took part in several mergers and acquisitions, company
sales, private placements, strategic alliances and business valuations.
More specifically, he acted as the principal financial advisor in
several acquisitions, including Technilab Pharma (acquired by Merckle
GmbH) and Draxis Health (TSE: DAX), as well as in a number of divestitures.
Prior to that, he occupied various commercial and management positions
with the Royal Bank of Canada, including three years as head of
the Montreal Life Sciences Group during which time he put in place
new financing for several companies in this sector.
Mr. Cantin holds a Master of Business Administration,
with a major in Finance, from the École des Hautes Études
Commerciales and a Bachelor of Education, with a major in Exercise
Physiology, from McGill University. He is also a graduate of the
Canadian Securities Institute.
Board Participation: Angiogène,
Chronogen, Eximias Pharmaceuticals
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Prior to joining Chipscreen, Dr. Zhang was the Managing
Director at Delirium, a global strategic consulting company in New
York. Dr. Zhang was a senior consultant at KPMG LLP's New York office
before Delirium. Prior to joining KPMG, Dr. Zhang also worked for
investment bank Credit Suisse First Boston's investment banking
group in New York. Dr. Zhang was a co-founder of CDR Therapeutics,
Inc., a Seattle-based bio-pharmaceutical startup that develops products
for the treatment of AIDS, psoriasis, corneal healing after laser
keratotomy, and breast cancer. Dr. Zhang is the inventor of several
U.S. patents and author of three nature biotechnology papers. Dr.
Zhang was awarded James A. McLaughlin Award from American National
Student Research Forum for his research in the Field of Immunology
and Infectious Disease. Dr. Zhang was also awarded Brupbacher Young
Investigator Award for his novel approaches to cancer therapy from
Charles Rudolph Brupbacher Foundation in Switzerland.
Dr. Zhang received his M.D. from Tianjin Medical
University. Dr. Zhang also holds a Ph.D. in pharmacology from the
University of Pennsylvania and an MBA from the University of Chicago
with a concentration in Finance and Accounting.
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Roger Feldman is a principal in the Corporate and
Securities Group of the national law firm of Fish & Richardson
P.C. Mr. Feldman has served as corporate counselor and advisor to
a broad range of clients from entrepreneurs, to maturing companies,
to major corporations. His practice is concentrated in corporate
finance, mergers and acquisitions, public and private securities
offerings, and general corporate transactions. Mr. Feldman has handled
all phases of business and corporate planning, structuring, and
organization; various phases of corporate finance (early and later
stage, including debt and equity); contract negotiations, strategic
alliances, and contractual and other commercial dealings; and stockholder
disputes. His practice is international in scope: he has been involved
in deal making throughout the world.
Mr. Feldman earned his law degree from Boston University School
of Law, where he was Articles Editor of the Boston University Law
Review. He earned his undergraduate degree cum laude from Harvard
College.
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Louis Myers, Ph.D., is a principal of the national
law firm of Fish & Richardson P.C. Dr. Myers counsels life sciences
clients on the formation and execution of intellectual property
strategies, usually in the context of over all business planning
and management including product development, technological issues,
competitive and collaborative relationships, financing strategies,
and the acquisition of technology, and other business considerations.
This can include patent drafting and prosecution; the provision
of infringement, validity, freedom-to-operate, and patent landscape
opinions; due diligence investigations; and drafting and analyzing
IP-related licenses and other agreements. Dr. Myers has worked in
most of the technologies and fields important to life sciences companies,
including basic molecular biology, geno /prote /pheno /chemo /glycomics,
bioinformatics, chip-array technologies, small molecule/organic
chemistry, drug discovery, gene and cell-based therapies, immunology,
antibody-based therapies and diagnosis, transgenic animals and plants,
DNA sequence analysis, nucleic acid detection and amplification
systems, the use of lasers in medicine and surgery, and medical
and biochemical instrumentation and devices.
Dr. Myers earned his Ph.D. in Biology from Harvard
University, where he also did his Postdoctoral work. He earned his
law degree from Harvard Law School. He has taught Patent Law at
Suffolk University Law School.
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Noubar B. Afeyan, Ph.D., Senior Managing Director
and CEO of Flagship Ventures, is a recognized technologist and entrepreneur.
With $600M under management, Flagship Ventures is a leader in creating,
funding and developing new ventures in both life science and information
technology sectors. Dr. Afeyan is also a Senior Lecturer at MIT's
Sloan School of Management and is a frequent guest speaker at technology
forums throughout the country. He has authored numerous scientific
publications and patents. He holds a Ph.D. in Biochemical Engineering
from the Massachusetts Institute of Technology.
Prior to co-founding Flagship Ventures in 1999, Dr. Afeyan co-founded
a number of successful ventures during his 13-year entrepreneurial
career. He was the Founder, Chairman, and CEO of PerSeptive Biosystems
(PBIO), a leader in the bio-instrumentation field that merged with
Applera Corp. (ABI) in 1998. During 1996 and 1997, he also served
as Chairman of the Board of ChemGenics Pharmaceuticals, a privately
held company spun out of PerSeptive and acquired by Millennium Pharmaceuticals
(MLNM) in 1997. Until August 1999, he was Senior Vice President
and Chief Business Officer of Applera Corporation, where he initiated
and oversaw the creation of Applera’s subsidiary, Celera Genomics
(CRA). He has also been a founding team member, investor and board
member of Antigenics (AGEN), Color Kinetics and EXACT Sciences (EXAS).
Dr. Afeyan currently serves as a Director for Flagship
portfolio companies Adaptive Therapeutics, Affinnova, Beyond Genomics,
Compound Therapeutics, engeneOS, Genstruct, and Helicos. In addition,
he serves on advisory boards for Boston University Medical School,
the Whitehead Institute at MIT, the McGowan Institute at the University
of Pittsburgh, the Center for Bits and Atoms at MIT’s Media
Lab, and the Faculty of Engineering at McGill University. He is
also a Board member of several economic development organizations
aimed at rebuilding the former Soviet Republic of Armenia.
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Senior Vice President, Life Sciences Investment BankingFriedman,
Billings, Ramsey Group, Inc. R. Nelson
Campbell is Senior Vice President and Head of Life Sciences Investment
Banking at Friedman, Billings, Ramsey & Co., Inc.
Prior to joining FBR in 2000, Mr. Campbell was the Chief Financial
Officer of EntreMed, Inc., a publicly-traded biotechnology company
based in Rockville, MD, from 1997 to 2000.
From 1991 to 1996, Mr. Campbell was the co-founder,
Vice President of Business Development and Treasurer of OsteoArthritis
Sciences, Inc., a venture capital-financed drug discovery company.
From 1986 to 1991, Mr. Campbell was engaged in corporate
finance and merger and acquisition transactions while working for
the international investment banking firms of Merrill Lynch Capital
Markets, Nomura Securities International, and Daiwa America Securities,
Inc.
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Jan van Heek joined Genzyme in 1991.
He is responsible for managing Genzyme's Therapeutics and Genetics
operations worldwide. He established Genzyme's European offices
and played a key role in developing the company's strategic vision.
Prior to joining Genzyme, Mr. van Heek held various management positions
at Baxter Healthcare Corporation in Europe and the U.S. for over
a decade. At Baxter, his last position was as vice president/general
manager of the global Fenwal Division of Baxter Healthcare Corporation
based in Deerfield, Illinois.
Mr. van Heek received a M.B.A. from St. Gallen University, Switzerland
and an executive degree from Stanford Business School, California.
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Dr Hans Küpper has over 30 years of experience
in the field of biotechnology in areas from research up to R&D
management, technology assessment and business acquisitions. He
received his PhD at the University of Heidelberg in 1974. After
additional academic research at the Massachusetts Institute of Technology
and Heidelberg University he joined Biogen, Geneva, where he held
various R&D positions, the last as Assistant Research Director.
In 1985, he joined Behringwerke AG, Marburg, to head its Molecular
Biology Department. Since 1991, he was increasingly involved in
deal negotiations and various aspects of company restructuring such
as acquisitions, spin-offs and joint ventures. In 1999, he joined
Global Life Science Ventures, Munich and is board member of several
portfolio companies. Dr Küpper is author of numerous publications
and served as consultant to the Pharmaceutical Industry and the
European Commission.
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As President of GMCG, LLC, Mark is a leading investment
banker to international public and private life science companies.
He has a successful history of cross border mergers and acquisitions
and cross border joint ventures. Mark has significant expertise
in the US listing process and in all forms of financing available
to domestic and international companies. He leverages his extensive
contacts both on Wall Street and in the international financial
markets to arrange and maximize financial opportunities for our
clients with market makers, international traders, institutional
public and private funds and high net worth investors. Mark holds
a JD from New York Law School and is a member of the New York Bar
Association.
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Mr. Stento joined the Firm in 1998. He was previously
a Managing Director at Comdisco Ventures, where he provided equity
and debt capital to startup and emerging growth technology and life
sciences companies. Prior to joining Comdisco, Mr. Stento was a
General Partner at Horsley Bridge Partners where he was responsible
for making and managing investments in a variety of private equity
partnerships and companies. Mr. Stento also spent six years in marketing
and sales at NCR Corporation, where he focused on information technology
solutions for financial institutions. Mr. Stento received a bachelor's
degree, with distinction, from Cornell University and an MBA from
Harvard Business School. He serves on several advisory boards including
Canaan Partners, Healthcare Ventures, Heritage Partners, Polaris
Venture Partners, Redpoint Ventures and Versant Ventures.
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Richard E. Kuntz is the Founder and Chief Scientific
Officer of the Harvard Clinical Research Institute (HCRI), a leading
CRO located within the unique world-class patient care and research
environment of the Harvard Medical School and affiliated institutions.
He is Associate Professor of Medicine at Harvard Medical School,
the Chief of the Division of Clinical Biometrics at the Brigham
and Women’s Hospital and an interventional cardiologist in
the Division of Cardiovascular Diseases at the Brigham and Women’s
Hospital.
Dr. Kuntz received his medical degree from Case Western Reserve
University and completed his residency in Internal Medicine at Parkland
Memorial Hospital, University of Texas Southwestern Medical School,
Dallas, Texas, and also served as chief medical resident. During
his Cardiovascular Fellowship training at Beth Israel Hospital and
Harvard Medical School, he received a master degree in Biostatistics
from the Harvard School of Public Health. Dr. Kuntz has directed
over 100 multicenter clinical trials involving more than 45,000
patients and has authored more than 200 publications. His expertise
in trial design and biostatistics is well-known in industry, academic
and government circles.
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Prior to joining OTL, Prem was Associate Director
of the Office of Industrial Affairs at Memorial Sloan Kettering
Cancer Center, and was Director of Business Development for Cadus
Pharmaceuticals of Tarrytown, NY from 1996 until 1999. He worked
with a start-up biotechnology company for several years prior to
joining Cadus, first as Director of Research and subsequently as
President and acting CEO. He has also worked as a business development
consultant in the biochip area. Prem received his Ph.D. in 1980
from the Chemistry Department at MIT and has academic research expertise
in several areas of modern biology.
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John leads the Imperial Innovations team with responsibility
for projects arising from the Faculties of Medicine and Life Sciences.
Imperial College’s medical school is one of Europe’s
largest and has close links with five major NHS hospital trusts
in the West London area.
Prior to joining Imperial Innovations, John worked
in a variety of strategy, business and corporate development roles
for GlaxoSmithKline, including responsibility for the divestiture
of Affymax by GSK. His early career began as a management consultant
with PricewaterhouseCoopers, before moving to Vernalis and taking
responsibility for R&D finance.
John sits on the board of directors of Sterix and
Harefield Cardiac and has close links with other Imperial College
spin-outs including Synovis and Protexeon.
John has a first degree in Natural Sciences (Biochemistry)
from University of Cambridge, supplemented with a D.Phil from University
of Oxford in Molecular Biology. He is a member of the Chartered
Institute of Management Accountants.
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Steven H. Holtzman is a founder and the President
and Chief Executive Officer of Infinity Pharmaceuticals, Inc. He
previously was the Chief Business Officer of Millennium Pharmaceuticals,
Inc. (NASDAQ: MLNM), the founder and Executive Vice President of
DNX Corporation, the founding Executive Director of the Ohio Edison
Program, and an instructor in moral philosophy and the philosophy
of language at Corpus Christi College, Oxford University, U.K. Mr.
Holtzman co-founded and from 1995-2000 was the Co-Chair of the Biotechnology
Industry Organization (BIO) Bioethics Committee. From 1996-2001
he was a member of the National Bioethics Advisory Commission; he
has served as a member of several NIH and NAS advisory committees
pertaining to the ethics of life science research; and, he is a
Trustee of The Hastings Center for Bioethics. Mr. Holtzman received
his B.A. in Philosophy from Michigan State University and his B.Phil.
graduate degree in Philosophy from Oxford University, which he attended
as a Rhodes Scholar.
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Graduate in Biochemistry, Genetics and Post Graduate
in Strategic Business Management of the European School of Management
(ESCP-EAP) Paris – France.
His experience comprises 19 years of International
sales, Marketing and Business Development.
Former Strategic Marketing Director for Sanofi Diagnostics
Pasteur, Beckman and Bio-Rad he is, since September 2000, the Director
of the Office of Technology Transfer at Institut Pasteur in charge
for the licensing of Diagnostics, Vaccines and Therapeutics patents.
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Mario Gobbo is in charge of Life Sciences investments
for IFC. He previously worked with Lazard Brothers in London where
he managed their Central and Eastern European practice. He began
his career as a commercial and later an investment banker in Milan
and London with several financial institutions.
He has over 20 years of banking experience, which
spans pharmaceuticals and biotechnology, as well as oil and gas,
telecommunications, power and financial institutions. He worked
on the initial public offering of Ares Serono, now Serono, the largest
European biotech company, and of Pliva from Croatia, the most prominent
pharma company in Central Europe. He also was on the board of a
small US biotech start-up and personally invested in several biotech
companies.
He holds a BA from Harvard College, an MSc from
the University of Colorado and an MBA and a PhD in finance from
the Wharton School of the University of Pennsylvania.
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After 30 years as a successful CEO, entrepreneur,and
operational manager, Stan Yakatan has dedicated the last 7 years
of his career to sharing his experiences with management teams interested
in building technology based companies. His experience as an executive
and in several instances serving as CEO with New England Nuclear,
EI Dupont, ICN Pharma, New Brunswick Scientific and Biosearch, provided
him with management and corporate finance acumen that he enjoys
sharing with others. He has founded or co-founded in excess of 15
companies in the United States, Canada, Israel, France and Germany
and in many cases served as the initial CEO, and Chairman of these
companies. He currently sits on the board of directors of several
public and private companies and has advised several of the world's
leading venture capital firms including TVM (Germany), Ventana (USA),
MSP (USA) and Biocapital (Canada). He has completed and advised
on numerous acquisitions and corporate finance transactions raising
in excess of $1.0 billion dollars in the public and private capital
financing markets. He is a frequent speaker at financial and biotechnology
conferences throughout the world speaking on topics including, "Capital
Raising for the Technology-Based Start-Up" and "The Need
to be Global in the Quest for Capital and Partners". Rick Biondi,
Editor of Lab Business Magazine stated," Mr Yakatan is a venture
capital raising Guru and it is part of his genetic make up."
He currently serves as the strategic advisor to the state government
of Victoria, Australia and is the Chairman of Katan Associates International
with headquarters in New York City.
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Eileen Smith Ewing represents biotechnology and
high-technology clients in intellectual property licensing and technology
transfers. In addition to a complex transactional practice, she
provides ongoing counsel to corporations, partnerships, and limited
liability companies on a wide range of legal matters. Ms. Ewing
also provides her private and public companies in domestic and transnational
mergers, acquisitions, joint ventures, and other strategic corporate
alliances. She has experience in counseling issuers, underwriters,
and venture capital funds with respect to public offerings and private
placements of securities.
Ms. Ewing lectures and writes frequently with respect to the life
science industries. She is a Contributing Editor of The Journal
of Biolaw and Business, to which she contributes regular articles
on legal topics affecting biotechnology. American Lawyer Media has
asked Ms. Ewing to serve as General Editor of its textbook on biotechnology
transactions, currently in preparation. Ms. Ewing is also currently
authoring the current supplement volume to the American Law Institute/American
Bar Association’s treatise on mergers and acquisitions.
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Lita Nelsen is the Director of the Technology Licensing
Office at the Massachusetts Institute of Technology, where she has
been since 1986. This office manages over 400 new inventions per
year from M.I.T., the Whitehead Institute, and Lincoln Laboratory.
Typically, they negotiate over 100 licenses, and start up over 20
new companies per year.
Ms. Nelsen earned B.S. and M.S. degrees in Chemical
Engineering from M.I.T. and an M.S. in Management from M.I.T. as
a Sloan Fellow.
Prior to joining the M.I.T. Technology Licensing
Office, Ms. Nelsen spent 20 years in industry, primarily in the
fields of membrane separations, medical devices, and biotechnology,
at such companies as Amicon, Millipore, Arthur D. Little, Inc.,
and Applied Biotechnology.
Ms. Nelsen was the 1992 President of the Association
of University Technology Managers and serves on the board the Mount
Auburn Hospital, and the Scientific Advisory Board of the Children’s
Hospital Oakland Research Foundation. She serves as the intellectual
property advisor to the International AIDS Vaccine Initiative and
is a founding and current board member of the Center for Management
of Intellectual Property in Health Research.
Ms. Nelsen is widely published in the field of technology
transfer and university/industry collaborations and was a CMI Fellow
at the University of Cambridge with the Cambridge MIT Institute
studying university /industry/ government partnerships in technology
transfer and local economic development. She is a co-founder of
Praxis, the UK University Technology Transfer Training Programme.
Contact info: Email: lita@mit.edu
MIT Address: NE25-230 (Five Cambridge Center)
To make appointments: call Andrea Barry, assistant to Lita Nelsen,
617-253-6966.
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Dr. Scolnick is President Emeritus, Merck Research
Laboratories. From 1982 to 2003, Dr. Scolnick served in multiple
capacities as President, Merck Research Laboratories and Executive
Vice President for Science and Technology, Merck & Company,
Inc; Executive Director and Vice President, Department of Virus
and Cell Biology, and Senior Vice President, Basic Research, Merck
Research Laboratories. Prior to joining Merck, Dr. Scolnick worked
at the National Cancer Institute where his work demonstrated the
cellular origin of sarcoma virus oncogenes in mammals and defined
specific genes that cause human cancer. He also worked at the National
Heart Institute where his work defined the stop signals in the genetic
code and the biochemical mechanism that produces the stops. Dr.
Scolnick was elected to the National Academy of Sciences in 1984
and to the American Academy of Arts and Sciences in 1993. He became
a member of the Institute of Medicine in 1996 and served on the
Board of Directors of Merck & Co., Inc. from 1997 - 2002. He
recently was selected as Regents’ Lecturer, University of
California Berkeley, Frank H.T. Rhodes Class of ’56 University
Professor at Cornell University, and appointed to the Board of Visitors
at the University of Pittsburgh School of Medicine. He currently
serves on the Board of Directors for Millipore Corporation, Renovis,
Inc., Harvard Medical School, Protein Pathways, TransForm Pharmaceuticals,
Inc., Medical and Scientific Advisory Board for MPM Capital, Hypnion,
and Protemix. He was also a Member of the FDA Science Board from
2000 - 2002. Dr. Scolnick’s commitment to the mental health
field is evidenced by memberships on the Board of Directors for
McLean Hospital, McGovern Institute for Brain Research, and is President
of the Pennsylvania Montgomery County Chapter of the National Alliance
for the Mentally Ill. He is also a board member of the National
Institute of Mental Health Council. Dr. Scolnick holds an A.B. from
Harvard College and a M.D. from Harvard University Medical School..
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Robert Mulroy is a President & CEO of Merrimack
Pharmaceuticals, Inc. Founded by leading scientists from MIT and
Harvard, Merrimack is focused on the discovery and development of
novel therapeutics for cancer and autoimmune diseases. The Company's
competitive advantage is its Network BiologyTM discovery
platorm: an integrated technology, biology, and computing capability
to profile the complex protein-protein interactions that govern
cellular pathways. The Company's lead product is currently in a
patient study of rheumatoid arthritis with three others in various
stages of research and development. Mr. Mulroy previously served
as CEO of Atlantic BioPharmaceuticals and as a strategy consultant.
He completed his undergraduate degree at Stanford and graduate work
at Yale.
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Ian Nisbet, Ph.D. works at Millennium Pharmaceuticals,
Inc. (MPI) where he is currently Senior Director, Oncology Alliance
Management and EU Strategic Marketing. In this role Ian is responsible
for managing the global VELCADE strategic alliance between Millennium
and the J&J family of companies, with particular emphasis on
the EU interface. Prior to this role, Ian was Product Leader for
VELCADE, where he led the team that was responsible for obtaining
FDA approval and launching this novel oncology drug in May 2003.
Ian originally joined Millennium through its then
subsidiary, Millennium BioTherapeutics (MBio), as Program Director
for the Therapeutic Antibody Program in February 1998. When MBio
was merged into MPI in December 1999, Ian moved into the position
of Senior Director, Licensing and M&A in Millennium’s
Corporate Development group. In this role, Ian supported Millennium’s
extremely aggressive growth objectives through the development and
implementation of strategic M&A and licensing initiatives. During
2001, Ian was a key member of the team that successfully negotiated
Millennium’s first two in-licensed clinical products (both
oncology drugs). In the same year, Ian led the diligence team for
Millennium’s acquisition of COR Therapeutics and then went
on to lead the merger integration team and become the site manager
for Millennium San Francisco (the ex-COR site). Upon returning to
Boston in mid-2002, Ian moved on to the VELCADE project.
Before joining Millennium, Ian worked for the Australian
pharmaceutical company CSL Limited in a career spanning more than
17 years. At CSL Ian held a number of different scientific and management
positions, the last being Director, Planning and Coordination. In
that position Ian was responsible for the development and implementation
of project management at CSL, together with overall management of
CSL’s project management system and direct management of a
number of CSL’s external relationships.
Ian received his B.Sc. in microbiology and biochemistry
from the University of Melbourne and his Ph.D. in molecular biology
from Monash University. He is also a graduate of the Advanced Management
Program from the Melbourne Business School at the University of
Melbourne.
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Mr. Mast is a Managing Director of Monument Group,
a specialized placement agent dedicated to representing superior
private equity and alternative investment opportunities. Prior to
joining Monument Group in February 1996, was a Consultant at Cambridge
Associates, Inc., where he specialized in working with a variety
of the firm's institutional and family group clients on alternative
asset investing. Prior to joining Cambridge Associates, Mr. Mast
had been Vice President at Venture Economics Information Services,
a division of Securities Data Company, Inc. where he worked internationally
with institutions and governmental entities designing and helping
implement private equity investment programs. His former work experience
includes a variety of management positions at Standard Oil Company,
Oceaneering International Inc., and Schlumberger Ltd. Mr. Mast has
a B.S. in Chemical Engineering from Princeton University and a M.B.A.
from Harvard Business School.
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Dr. Ansbert Gadicke is the Founding General Partner
of the MPM Group. He led MPM's effort to build its Advisory and
Investment Banking business from 1992 to 1996 and started its Asset
Management business in 1996. Prior to founding MPM, Dr. Gadicke
was employed by The Boston Consulting Group.
Dr. Gadicke received an M.D. from J.W. Goethe University
in Frankfurt. He subsequently held research positions in biochemistry
and molecular biology at the Whitehead Institute at MIT, Harvard
University and the German Cancer Research Center. He has published
in leading scientific publications including Nature and Cell. Dr.
Gadicke is Chairman of Elixir and a Director of Arriva, Endeavor
Pharmaceuticals, Kourion, Idenix Pharmaceuticals, Omrix Biopharmaceuticals,
Pharmasset, and ViaCell. He previously served as a Director of BioMarin,
Coelacanth, MediGene and Transform. He is a member of Advisory Councils
for Harvard Medical School, the Health Science and Technology Program
of Harvard and MIT, as well as the Whitehead Institute at MIT. He
serves as the Co-Chairman of the Alumni Association of the Whitehead
Institute and serves on the Board of the National Venture Capital
Association (NVCA).
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Primary responsibilities include strategic planning,
intramural and extramural technology transfer policy, legislative,
international and governmental affairs. Also has oversight responsibility
for license monitoring and royalties administration activities.
Serves as the Executive Secretary for the Public Health Service
Technology Transfer Policy Board. Holds advanced degrees in Counseling
Psychology and Public Health, awarded the designation as a Certified
Research Administrator, and has authored a number of articles in
professional and refereed journals..
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Otello joined NIB Capital in 2001 from Lombard Odier,
where he managed the Immunology Fund, one of the world's largest
funds investing in US and EU public and private Biotechnology companies.
Previously, he was at Goldman Sachs in London in their HealthCare
corporate finance and M&A group. Prior to that, he started the
Life Sciences activity of Index Securities (now Index Ventures),
in Geneva. Graduated from Geneva University with a PhD degree in
Molecular Biology, and with an European PhD in Biotechnology, Otello
brings to portfolio companies a strong scientific background but
also the understanding of public and private healthcare markets,
specialized knowledge of Biotech Intellectual Property, and transaction
experience.
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Sam’s coverage is mainly focused on UK small
and mid-cap biotechnology companies. In the near future coverage
will be expanded into continental Europe while maintaining a focus
on biotechnology. Sam has been covering the UK and European sectors
for the past 7 years. His background as a pharmacologist with extensive
post-doctoral experience of molecular biology and genetic sciences
has positioned him well to judge the scientific merit and commercial
potential of new technologies and products.
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Jeremy is the Global Head of Strategic Alliances
for Novartis Institutes.
In this position Jeremy is responsible both for
evaluating and managing current alliances with academia and biotechnology,
interfacing with the venture community and establishing strategic
collaborations to further the research mission of NIBR.
From 1996 to 2000, Jeremy served as the Chairman
of Physiome Sciences, Inc., and was appointed as Physiome's President
and Chief Executive Officer in 2000. From 1998 through 1999 he was
Managing Director of Perseus Capital LLC and from 1992 to 1998,
Jeremy served as the President and Chief Executive Officer of Cadus
Pharmaceutical Corporation, where he also served as Chairman from
1996 to 1998. Prior to 1992, Jeremy was a Vice President at IG Laboratories,
a wholly owned subsidiary of Genzyme Corporation. In these positions,
Jeremy developed and lead multiple collaborations with partners
from academia, biotech through to major pharmaceutical companies.
Jeremy has served on the Executive Committees and
Boards of several public biosciences companies, including the executive
committee of BIO and the Boards of the Biotechnology Institute and
the New York Biotechnology Association. Jeremy received an MB.BChir.
from the University of Cambridge and a D.Phil. in DNA structure
from the University of Oxford.
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Michael Lytton joined Oxford Bioscience Partners
in 2000. Prior to that, he was Partner, Chairman of the Technology
Group and a member of the Executive Committee of Palmer & Dodge
LLP, a Boston-based law firm. Mr. Lytton serves on the Boards of
Directors of Acambis, Alantos, Descartes Therapeutics, GPC Biotech,
Graffinity Pharmaceuticals, Rib-X Pharmaceuticals, and VaxInnate
Pharmaceuticals. Mr. Lytton was also responsible for investments
by Oxford in Concentric Medical, Genpath Pharmaceuticals, and NuVios
Pharmaceuticals. Mr. Lytton is also a member of the Research and
Technology Development Committees of the Beth Israel Deaconess Medical
Center (an affiliated Harvard teaching hospital) and the Center
for Blood Research, Harvard Medical School, where he is also a member
of the Board of Overseers. In addition, he serves on the Advisory
Committee to Connecticut Innovations, a public agency funding early-stage
biomedical companies in Connecticut. Mr. Lytton writes a column
on issues facing early-stage biomedical companies for Start-Up magazine,
published by Windhover Information. Mr. Lytton has served on the
Executive Board of the MIT Enterprise Forum and the Patent Committee
of the Boston University Medical Center. Mr. Lytton was a summa
cum laude graduate of Princeton University and a recipient of a
Fulbright Scholarship for study at the University of London. Mr.
Lytton received a J.D. degree cum laude from Harvard Law School.
Mr. Lytton also received a M.Sc. degree in Epidemiology and Medical
Statistics from the London School of Hygiene and Tropical Medicine.
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Dr. Kiron has been at Pfizer since 1991 contributing
to drug discovery in the Cardiovascular & Metabolic Diseases
Department. He obtained experience in drug development in the Project
Management Department shepherding the progress of a discovery stage
compound through early phases of clinical development. Dr. Kiron
earlier earned a B.Sc. in Chemistry and a M.Sc. in Microbiology
from Bombay University and a Ph.D. in Biochemistry from the Indian
Institute of Science in Bangalore, India. Dr. Kiron then came to
the Cardiovascular Center of Cornell University Medical Center-The
New York Hospital, New York, NY where he stayed on to hold joint
appointments as a tenure track Assistant Professor of Biochemistry
and Medicine. He came to Pfizer from Cornell and earned his MBA
degree from Rensselaer (RPI) at Hartford, CT.
Dr. Kiron is an experienced pharmaceutical industry
scientist and strategic analyst with significant experience in management,
leadership and problem solving. He has diverse experience and a
broad perspective of the various processes of pharmaceutical drug
discovery, pre-clinical and early clinical drug development, project
management, external technology investments and licensing. Dr. Kiron
also managed until recently the discovery protein outsourcing activities
as well as the licensing of research tools for research in genetic
therapies and genomics. His current responsibilities include business
and competitive analysis of the biotechnology and pharmaceutical
industry, providing insight into their strategies and benchmarking
their activities. Dr. Kiron also participates in the analysis of
new technology opportunities, potential pharmaceutical and biotechnology
Mergers & Acquisition opportunities for Pfizer and is involved
in strategic planning for future collaborations.
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Christoph H. Westphal is a general partner in our
Boston office. Christoph joined Polaris in June 2000. He focuses
on investment opportunities in medical technology and material science.
Experience: Prior
to joining Polaris, Christoph was at McKinsey & Co. in Boston
and Los Angeles, working with high-growth biotech, pharmaceutical,
materials science, wireless, and e-commerce companies. He was lead
author on several papers published in Cell and Nature Genetics and
is the inventor on two patents in the areas of cancer genetics and
metabolic diseases.
Boards: Christoph
represents or has represented Polaris on the boards of directors
of Advion BioSciences, Athenix Corp, Saegis Pharmaceuticals, eNOS
Pharmaceuticals, Hydra BioSciences, and Nanosys. He was also founder
and start-up CEO, and serves as vice chairman of both Momenta Pharmaceuticals,
Inc. and Alnylam Pharmaceuticals.
Education: Christoph
completed his MD at Harvard Medical School and his PhD in genetics
at Harvard University in six years. He majored in economics, literature,
and biology while completing a BA summa cum laude and Phi Beta Kappa
at Columbia University in three years. After graduating from Columbia,
and prior to graduate schools, Christoph spent one year working
with a medical team and studying in Cameroon and at the Albert Schweitzer
Hospital in Africa, and worked for one year at a Max Planck Institute
in Germany as a Fulbright/DAAD scholar.
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James joined SVLS in May 1995 as Chief Executive
Officer and Managing General Partner of SVLS, overseeing its approximately
$900m investment activity. James brings a successful healthcare
investment track record, preceded by 18 years of operating management
experience. Prior to joining SVLS, he was Managing Director for
the $600m Venture Capital Division of Allstate Corporation preceded
by managing Allstate’s health care investment activity. He
has held several senior management positions in companies with multinational
operations including Kendall (TyCo) & Millipore. He was also
president of start-ups Allegheny International Medical Technology
and National Teledata. James has served on the boards of private
and public companies in the US and Europe including public companies
Alscript Pharmaceuticals, Arris Pharmaceuticals, LaserVision Centers,
Orthovita, Shire Pharmaceuticals and SunRise Assisted Living.
James received a BS degree from Northern Illinois University in
1969.
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Dr. Stelios Papadopoulos is a Vice Chairman of SG
Cowen and as an investment banker he focuses on the biotechnology
and pharmaceutical sectors. Prior to joining SG Cowen in February
2000, he spent 13 years as an investment banker at PaineWebber,
Incorporated where he was most recently Chairman of PaineWebber
Development Corp., a PaineWebber subsidiary focusing on biotechnology.
He joined PaineWebber in April 1987 from Drexel Burnham Lambert
where he was a vice president in the Equity Research Department
covering the biotechnology industry. Prior to Drexel, he was a biotechnology
analyst at Donaldson, Lufkin & Jenrette.
Before coming to Wall Street, Dr. Papadopoulos was on the faculty
of the Department of Cell Biology at New York University Medical
Center. He continues his affiliation with NYU Medical Center as
an Adjunct Associate Professor of Cell Biology. Dr. Papadopoulos
holds a PhD in biophysics and an MBA in finance, both from New York
University.
Dr. Stelios Papadopoulos is a co-founder and Chairman
of the Board of Exelixis, Inc., and he is a co-founder and member
of the Board of CellZome, Inc. and Anadys Pharmaceuticals, Inc.
He is also a member of the Board of Directors of GenVec, Inc. and
Structural GenomiX, Inc. In the not-for-profit sector, Dr. Papadopoulos
is a co-founder and Chairman of Fondation Santé.
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Antoine Papiernik is managing partner at Sofinnova
Partners and invests in life sciences. He joined Sofinnova Partners
in 1997.
Antoine has an MBA from the Wharton School (University
of Pennsylvania). He began his career in London as product manager
at Unilever ’s Health & Beauty division. He then spent
four years in Prague, first as a consultant, then as an investor
for CDC-Participations (Caisse des Dépôts Group). He
then moved to the newly formed venture capital firm CDC-Innovation,
where he invested exclusively in life sciences.
Antoine was an initial investor and board member
of Actelion, a Swiss biopharmaceuticals company that is now listed
on the Zürich stock exchange. He has also invested in and is
a board member of NovusPharma, Diatos, SpineVision, EndoArt, Biolipox,
Promed and Addex.
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N. Peter Kostopulos is a partner in the Life Sciences
Group of the law firm of Womble Carlyle Sandridge & Rice, and
the leader of its BioAlliance Practice, a multi-disciplinary, industry-oriented
group, which provides bio-pharma clients with legal and related
business transaction support for their corporate partnering activities.
For 15 years, Peter has represented private and venture-backed development
companies on a variety of R&D and commercial alliances involving
drug, diagnostic and medical device products. He has been particularly
active in transatlantic transactions, providing European and American
clients with assistance in negotiating and closing transactions
with large pharmaceutical and biotech companies in the United States
and Europe. Peter has participated in over 75 domestic and international
collaborations and intellectual property transactions, many of which
involved providing direct support to senior business development
management, steering committees and alliance managers. His substantial
litigation and previous government experience (FTC & Justice
Department) provides clients with valuable assistance in avoiding
and resolving costly litigation and government investigations. He
is Chairman of the Strategic Alliances Committee of the Licensing
Executives Society (USA/Canada), and has spoken at numerous U.S.
and European conferences and written on a variety of topics relating
to alliances, including early stage deal structuring, negotiating
with big pharma, organizing and managing the alliance, conducting
alliance due diligence, extracting value from and terminating R&D
alliances, and the antitrust guidelines for intellectual property.
He is a 1974 graduate of Georgetown University and 1978 graduate
of the Georgetown University Law Center, and is a member of the
bars of Washington D.C., Florida, Maryland and Virginia. He speaks
French, and has lived outside the United States.
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