Good Manufacturing Practices (GMP) Insights
CfPIE Insights from Industry Experts
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
This is a three-day course that provides a thorough dive into the foundations of manufacturing and distribution regulations for the medical and pharmaceutical industries in the United States.