On-Demand Webinars

Past Webinars

24 June, 2026
Medicinal Products,
Labeling
CCDS Implementation: Practical Strategies for Local Regulatory Labeling Alignment
March 31, 2026
Medicinal Products,
Regulatory Affairs
A Regulatory Guide to DMF Submissions in China: APIs, Excipients & Packaging Materials Explained
October 3, 2025
Medicinal Products,
Regulatory Affairs
Navigating US FDA IND Submissions: Non-clinical Requirements and Compliance for Research and Testing Facilities and Communications with US FDA
September 24, 2025
Medicinal Products,
Artwork
Centralization of Artwork Operations through Shared Services
March 27, 2025 
Medicinal Products,
Regulatory Affairs
Innovative Drug Development in China
December 05, 2024
Medicinal Products,
Regulatory Affairs
Critical Timelines for EU CTR Implementation - Are you prepared?
November 6, 2024
Medicinal Products,
Labeling
ePI FHIR Labeling: Understanding the Importance, Guidelines, and Challenges
October 15, 2024
Medicinal Products
Overview of PMDA Clinical Trial Consultation
October 9, 2024
Medicinal Products
Achieve Perfection in Pharma Ad Promo Communications Effective MLR Compliance Practices
September 26, 2024
Medicinal Products,
Regulatory Affairs
Strategic Guide for License Transfers in South Korea
August 29, 2024
Medicinal Products,
Publishing and Submission
Navigating eCTD Submissions in China
March 06, 2024
Medicinal Products,
Regulatory Affairs
Decoding China's Marketing Authorization Holder (MAH) System