Presented on December 3rd, 2019
Download the slide deck and video presentation of this informative 1-hour webinar on assessing legacy products for potential GMP compliance gaps and pitfalls. This session will be valuable to quality, regulatory, compliance, and management personnel in pharma companies that manufacture legacy products and want to ensure those products remain compliant. Key takeaways:
- Understand why it is important to assess legacy products for potential GMP compliance gaps.
- Learn where the most likely compliance pitfalls are and how to assess your legacy products.
Jerry Chapman
Senior GMP Quality Expert at Redica Systems
If you have any questions or comments or need help with the form, please do not hesitate to contact someone on our team at events@redica.com.