Pharma and Biopharma Quality System Refresher Course
Webinar
Quality System Training is mandatory per regulatory agencies, no matter where in the world you want to market your medicinal products including Pharmaceuticals and Biopharmaceuticals. Regulatory agencies are looking into seeing whether companies' Quality Systems are in control during License Renewal Inspections, Cause Inspections, System Based Inspections and Pre-approval (PAI) Inspections. Many companies are getting Warning Letters and or Consent Decree due to violations in Quality Systems requirements.
This session will train you in one of the eight major modules of ASQ cGMP Certification Training Program for Pharma and Biopharma. The presenter will share new information and industry best practices and provide ample opportunity to ask questions.
Attendees are highly encouraged to submit pre training questions. The instructor will make every effort to cover or answer most of the questions during the presentation or during Q&A the session.
(Courtesy of Pharmaceutical products, via en.wikipedia.org)
Fri, Jan 11, 2013 - Fri, Jan 11, 2013
Online Event
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