Services

  • Legal advice and counseling on federal and state laws governing the conduct of clinical research.
  • Negotiation of clinical trial agreements, CRADAs and other technology transfer agreements for drugs, medical devices and dietary supplements.
  • Development and negotiation of contractual agreements and other administrative and regulatory documents such as investigator and site agreements.
  • Consultation on the clinical development process, including human subjects protection issues, such as recruitment practices and informed consent.