Life Science Collaborations and Clinical Trials
Our attorneys have served as both outside and in-house counsel for life science companies, and our attorneys understand the range of complex legal, competitive, and operational issues facing such companies. Our extensive IP experience
and our understanding of various healthcare-related statutes and regulations such as Stark Law, PhRMA code, FDA,
OIG guidances, False Claims Act, anti-kickback, anti-bribery laws, HIPAA, privacy, security, and data breach issues helps
us navigate challenging contract issues, effectively representing client interests in clinical trial agreements and other complex negotiations.
Our current range of legal services includes analyzing, negotiating, and drafting:
and our understanding of various healthcare-related statutes and regulations such as Stark Law, PhRMA code, FDA,
OIG guidances, False Claims Act, anti-kickback, anti-bribery laws, HIPAA, privacy, security, and data breach issues helps
us navigate challenging contract issues, effectively representing client interests in clinical trial agreements and other complex negotiations.
Our current range of legal services includes analyzing, negotiating, and drafting:
- U.S. and global clinical trial agreements and informed consent documents for domestic and international clinical trials
- Manufacturing, quality, and supply agreements
- CRO agreements, laboratory services agreements, distribution and sales agreements, and services agreements
- Nondisclosure, consulting, and employment agreements
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