About
Practicing at the forefront of the life sciences industry, Anisa Mohanty advises medical device, biotech and pharmaceutical companies on US Food and Drug Administration (FDA) premarket strategy and post-market compliance issues, from advertising and promotion to disclosure and periodic reporting. Her experience encompasses such matters as premarket pathways, Good Laboratory Practice and Good Clinical Practice and Good Manufacturing Practice (cGMP) and Quality System requirements. Read full biography: https://www.mwe.com/people/mohanty-anisa/
Overview
Practice focus
Firm
Office details
Location
Washington, DC 20001
Services
Practice areas
Languages
Reviews
Be the first to leave a review
Share your experience
No reviews yet
Be the first to share your experience working with Anisa.
Is this your profile?
Claim it to update details and respond to leads.
Credentials
No credentials have been added to this profile yet.
