SRC is a team of highly experienced, industry professionals with expertise in product development, clinical, and regulatory expertise in the drug, and medical device areas and medical communications.
The Safety and Regulatory Affairs Team of SRC includes expertise in the areas of Regulatory Affairs, as well as nonclinical pharmacology and toxicology, pharmacokinetics, and clinical development. The Medical Communications and Project Management Team manages all efforts related to clinical trial design, project management, and scientific and regulatory writing.
Specialties
Gap analyses, regulatory consulting, FDA meeting management, medical writing
