ResearchBib Share Your Research, Maximize Your Social Impacts
Sign for Notice Everyday Sign up >> Login

Risk Management 2020 - Pharmaceutical Quality Risk Management

Date2020-09-10

Deadline2020-09-10

VenueOnline, Online Online

Keywords

Websitehttps://worldcomplianceseminars.com/p/ph...management

Topics/Call fo Papers

Risk is everywhere. And growing. When you consistently apply appropriate QRM principles and tools, you’ll stay compliant. But if you’re struggling to manage the types — and severity — of risk with your Quality Risk Management (QRM) techniques, problems proliferate.
You’re probably exerting a huge effort: QRM must be applied consistently to an ever-increasing roster of drug development, manufacturing, distribution, and inspection and submissions review processes.
Best practices related to QRM program development and execution, including process, people and documentation
Ways to integrate QRM into your quality systems such as change control and investigations and how integration can benefit your organization
Explore the PIC/S Aide-Memoire on QRM and how you can prepare for an inspection of your QRM program
Speaker:
Ms. Thomas has over two decades of cGMP hands-on industry experience in both pharmaceutical and medical device manufacturing operations.

Last modified: 2020-09-10 21:29:23