Good Manufacturing Practices (GMP) Insights
CfPIE Insights from Industry Experts
Build a GMP-compliant QMS: step-by-step guidance on quality policy, roles, documentation, process control, training, and audits for continuous improvement.
Avoid GMP audit failures: learn to fix documentation, training, deviation control, cleaning protocols, and change management with proactive strategies.
Demystify global GMP standards: compare FDA, EU, WHO guidelines, harmonization efforts, and key similarities to keep your compliance strategy sharp worldwide.
Explore GMP vs GLP differences. Discover how integrating both frameworks enhances compliance, safety, quality, and drives success across life sciences.
Current Good Manufacturing Practices are a set of compliance regulations for drug manufacturers and pharma companies to ensure the quality of their products.
Learn about the 5 key components that help pharmaceutical companies in the United States manufacture medications that are safe and effective, while adhering to the cGMP regulations set by the FDA.
Good Manufacturing Practices are the processes designed to ensure products are consistently made according to the high standard set by the (WHO).
In December of 2018, the FDA released a report: Current Good Manufacturing Practice – Guidance for Human Drug Compounding Outsourcing Facilities Under Section 503B of the FD&C Act.
Learn how CMC Regulatory Compliance for Biopharmaceuticals & Biosimilars course from CfPIE is keeping you ahead of the curve on cell therapy, gene therapy, transgenic plant cell cultures and transgenic animals