ComplianceOnline, Online Event
2013-01-11
This 90-minute quality system requirements training will cover industry best practices, recent regulatory updates and practical tips on how pharmaceutical and biopharmaceutical companies can ensure their quality systems are in control and in compliance with agency expectations. Why Should You Attend: 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. Learning Objective: Attendees will gain a thorough understanding of Pharmaceutical and Biopharmaceutical Quality Systems and the associated requirements.
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