Full Name
Sarah Wicks
Job Title
Associate
Department
FDA/Life Sciences Practice
Company
Goodwin Procter
Speaker Bio
Sarah is an associate in Goodwin’s FDA practice where she counsels pharmaceutical companies on FDA regulatory compliance issues. She provides strategic advice on matters involving product development and marketing approval and negotiates the regulatory terms of clinical and research related agreements. She also advises on regulatory compliance with good clinical practices, including informed consent, adverse event reporting, trial initiation and monitoring, sponsor and investigator responsibilities, financial disclosures and data integrity.
Sarah Wicks