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 22, 2024
• 90 Minutes
• US$149.00
• Enroll

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 29, 2024
• 90 Minutes
• US$149.00
• 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

• May 1, 2024
• 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

• May 6, 2024
• 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

• May 9, 2024
• 3 Hours
• US$299.00
• 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

• May 13, 2024
• 90 Minutes
• US$149.00
• Enroll

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

• May 31, 2024
• 90 Minutes
• US$149.00
• Enroll