Creating and Maintaining a GMP Quality System 2016
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The webinar will discuss basic/key requirements for creating and maintaining a GMP compliant quality system in the FDA regulated industries.
In this webinar:
- You will gain the knowledge base for operating in a GMP compliant environment
- You will have a better understanding of the basic requirements that FDA seeks in the FDA regulated industries
- Speaker will layout the basic knowledge base for the top requirements for a GMP complaint quality management system (QMS)
Areas Covered in the Session :
- Good Manufacturing Practices – Overview
- Quality Management System – Overview
- Key requirements for creating an FDA compliant Quality Management System
- Prerequisites for meeting GMP compliance
- Interactive Q&A Session
Who Should Attend:
- Quality Assurance Professionals
- Quality Control Professionals
- Regulatory Professionals
- Pharma/Medical Devices/OTC Cosmetic Manufacturing Teams
- Pharma/Medical Devices/OTC Cosmetic Packaging Teams
- Pharma/Medical Devices/OTC Cosmetic Subcontractors
- Contract Testing Laboratories
- Owners/Presidents of GMP regulated companies
Course Director: JAN L. WARNER
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