Certified Pharmaceutical GMP Professional (CPGP) VECG Trainging

Regulatory Agency Governance -Quality Systems -Laboratory Systems -Infrastructure: Facilities, Utilities, Equipment -Materials and Supply Chain Management -Sterile and Non sterile Manufacturing Systems -Filling, Packaging, Labeling -Product Development and Technology Transfer

Objective

Preparing for and passing the CPGP exam greatly enhances the ability of a company’s GMP-following employees and management to raise the GMP compliance "bar" to a new level. - Supports internal continuous quality improvement programs. - It is sector-specific applied knowledge.

Who Should Attend

The Certified Pharmaceutical GMP Professional understands the GMP principles as regulated and guided by national and international agencies for the pharmaceutical industry. This covers finished human and veterinary drugs and biologics, ectoparasitacides, and dietary supplements (alternatively called nutraceuticals where regulated as drug products, as well as their component raw materials (includes active pharmaceutical ingredients (APIs) and excipients), and packaging, and labeling operations.

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