In the complex world of development to commercial distribution, each phase poses its own challenges in terms of providing assurance of the safety, efficacy and quality of the product being developed. Dossiers submitted to regulatory authorities need to include comprehensive data that meets specific requirements of that authority, a difficult task.

Join this webinar and discover:

• What health authorities are looking for in your submissions.
• How dossiers are compiled, written, and reviewed to meet all technical and quality standards.
• Ways Lonza’s global regulatory expertise reduces risk and speed time to market, and ensures right first time filings
• The support Lonza provides to customers beyond approval to maintain compliance throughout the product lifecycle.

This webinar is a much-watch for:

• Regulatory and Compliance Professionals
• CMC and Supply Chain Experts
• Outsourcing Experts

Sponsored by:

Speakers:

Roche Walliser
Senior Director, Head of Regulatory Affairs, Advanced Synthesis
Lonza

Praveenkumar Devakadaksham
Director, Regulatory Affairs, CMC, Advanced Synthesis,
Lonza