CfPIE Insights
CfPIE Insights from Industry Experts
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).
One of the most important times of the year for professionals engaged in Good Manufacturing Practices quality assurance, the annual product quality review as mandated by the FDA allows your business to ensure not only compliance with FDA regulations, but also ensure the best quality products that carry your brand name are on the market.
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.