
Julia Post
Professional Bio
Julia Post advises biotechnology, pharmaceutical, medical device, and trade association clients on a variety of federal and state regulatory and compliance matters. In particular, Julia has experience in areas including biosimilars and interpretation and implementation of the Biologics Price Competition and Innovation Act of 2009; human cells, tissues, and cellular and tissue-based products (HCT/Ps); market exclusivity; informed consent requirements; and pharmacy substitution practices.
Prior to joining the Food and Drug practice group, Julia was a member of the Litigation practice group where she focused on representing clients in Hatch-Waxman patent litigation.
FDA Releases Discussion Paper on AI in the Drug and Biological Product Development Process
Covington Digital Health ·
FDA Releases Draft Guidance on Electronic Systems, Records, and Signatures in Clinical Investigations
Covington Digital Health ·
Oregon HB 4005: New Reporting Requirements for Drug Manufacturers, Health Insurers
Inside Government Contracts ·