Certified Pharmaceutical GMP Professional (CPGP) Training
About Course
The Certified Pharmaceutical GMP Professional (CPGP) certification, offered by organizations such as the American Society for Quality (ASQ), is for professionals ensuring compliance with Good Manufacturing Practices (GMP) in pharmaceutical manufacturing. CPGP validates expertise in quality assurance, regulatory requirements, quality systems, and auditing principles specific to pharmaceutical production. Holders of CPGP demonstrate proficiency in maintaining high standards of product quality, safety, and efficacy, ensuring adherence to regulatory guidelines and continuous improvement in manufacturing processes. This certification enhances career opportunities by confirming skills in GMP compliance, quality management, and contributing to the safe and effective production of pharmaceuticals to meet global healthcare standards.
Course Content
Module 1: Introduction to Pharmaceutical GMP
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Chapter 1: Overview of Pharmaceutical GMP
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Chapter 2: Regulatory Framework for Pharmaceutical GMP
Module 2: Quality Management Systems in Pharmaceutical GMP
Module 3: Facility and Equipment Compliance in Pharmaceutical GMP
Module 4: Personnel and Training in Pharmaceutical GMP
Module 5: Documentation and Record Keeping in Pharmaceutical GMP
Module 6: Production and Process Controls in Pharmaceutical GMP
Module 7: Sterile and Non-Sterile Manufacturing in Pharmaceutical GMP
Module 8: Validation and Qualification in Pharmaceutical GMP
Module 9: Audits and Inspections in Pharmaceutical GMP
Module 10: Laboratory Operations and Pharmaceutical GMP
Module 11: Deviations, Non-Conformances, and Change Control in Pharmaceutical GMP
Module 12: Roles and Responsibilities of a Certified Pharmaceutical GMP Professional
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