This combined Quality Agreement and DMF (Drug Master Files) training will discuss the advantages for suppliers and drug product manufacturers developing these arrangements together.

Robert J. Russell

• April 2, 2026
• 90 Minutes
• US$149.00
• Enroll

The Latin America Regulatory compliance requirement training/webinar will cover topics across the full Life-Cycle of Company & Product licensing in the key markets of Latin America.

Robert J. Russell

• April 8, 2026
• 90 Minutes
• US$149.00
• Enroll

This 3-Hour webinar covers the details of the Regulatory Requirements for a wide-range of Life Science products in Japan: Pharmaceuticals, Biologics, Medical Devices and Combination Products.

Robert J. Russell

• April 13, 2026
• 3 Hours
• US$299.00
• Enroll

This course specifically focuses on the overall regulatory compliance requirements and procedures for Pharmaceuticals, Medical Devices, Biologics, and Combination Products in Japan.

Robert J. Russell

• April 17, 2026
• 90 Minutes
• US$149.00
• Enroll

This EU Medical Device Regulation (MDR) 90-minute webinar will discuss the recently developed regulation and its impact on the future compliance and registration of medical devices in the EU.

Robert J. Russell

• April 24, 2026
• 90 Minutes
• US$149.00
• Enroll