Regulatory and Compliance Webinar: APAC

This focused half-day webinar is designed for regulatory affairs professionals and compliance teams managing product registrations, safety dossiers, and labelling requirements across the APAC region. Sessions are presented by practising regulatory consultants with direct market experience.

Markets Covered

Sessions will focus on updated notification frameworks in China (NMPA), India (BIS), ASEAN harmonisation under the ASEAN Cosmetic Directive, and recent changes to Japan's Pharmaceutical and Medical Device Act as it applies to quasi-drug products.

Who Should Join

Regulatory affairs managers, legal counsel, quality assurance leads, and product managers responsible for market access in Asia. A live Q&A with the presenting consultants closes the session.