Hosted by Pharmceutical Executive, listen to former Director of the Office of Compliance for FDA CDER, Cynthia Schnedar and GM at Dot Compliance Mikey Landkof discuss the changinmg landscape of quality and compliance. Hear how new technologies and deployment methodologies are replacing the more traditional paper-based QMS systems.
Learn how new QMS technologies offer advantages over legacy and paper-based QMS solutions because they are easier and more cost effective to implement, and have built-in internal controls to ensure quality and compliance.
Attendees will learn:
- What key advantages pre-configured, ready to use QMS can provide to pharma manufacturers
- What key requirements pharma manufacturers must be compliant with when implementing an electronic-based QMS
- How it is possible to break down silos and improve quality by using comprehensive ready-to-use solutions that are properly validated