Description
Be a Better Life sciences Products Litigator or Patent Attorney.Develop greater securities and investment expertise in Your Field.
The approval process pre-approval concerns product labeling clinical trials adverse events reports patent concerns exclusivity. All are critical aspects in the commercialization process for drugs, biologics, and devices, which are governed by FDA law and regulation. Recent court cases and high-profile trials concerning FDA-regulated products have made it clear that it is essential for attorneys who do not have regulatory practices but who do deal with FDA-regulated products to have a familiarity with these concepts.
Attend this conference and learn to navigate your way through the regulatory maze that plays such a crucial role to your cases and practice areas.
