This 60-minute webinar on GMP Compliance for Biopharmaceuticals and Cell & Gene Therapy Products provides a comprehensive overview of regulatory expectations, quality management principles, and industry best practices for ensuring compliance in these highly specialized fields.

Charles H. Paul

• June 24, 2025
• 60 Minutes
• US$149.00
• Enroll

This webinar is about effective communication inside and outside of the project team. The webinar will use case studies and examples to reinforce key teaching points.

Charles H. Paul

• June 25, 2025
• 90 Minutes
• US$149.00
• Enroll

Post-Market Surveillance (PMS) and Vigilance Reporting for Medical Devices and Combination Products are critical components of regulatory compliance, ensuring ongoing patient safety and product effectiveness after market approval.

Charles H. Paul

• June 26, 2025
• 60 Minutes
• US$149.00
• Enroll

In today's fast-paced and highly analytical project environments, leaders often rely heavily on metrics, deadlines, and documentation to steer their teams.

Charles H. Paul

• July 1, 2025
• 60 Minutes
• US$149.00
• Enroll

In the highly regulated world of pharmaceuticals, biotechnology, and medical devices, project managers face constant pressure to deliver results on time while ensuring strict adherence to FDA compliance requirements.

Charles H. Paul

• July 3, 2025
• 60 Minutes
• US$149.00
• Enroll