The main market opportunity lies in the need for comprehensive GMP audits in the pharmaceutical industry. By integrating interviews with traditional methods, such audits provide deeper insights into ...

The "Golden Rules of Being a Successful GMP Auditor (September 30, 2026 and Oct 1, 2026)" training has been added to ResearchAndMarkets.com's offering. Navigating thorough and successful GMP audits ...

As discussed in the Product Perspective, the Modernization of Cosmetics Regulation Act of 2022 (MoCRA) represents a major shift in cosmetic industry regulations. This article is one of a series of ...

FDA recently published a Federal Register notice announcing a public listening session on good manufacturing practices (GMPs) for cosmetic products under the Modernization of Cosmetics Regulation Act ...

Regulators stress accountability: FDA and EU frameworks require sponsors to maintain oversight of CDMOs, treating outsourcing as an extension of the pharmaceutical quality system. Quality control as ...

Manufacturers are usually subjected to a diverse variety of regulations typically established by international and regional bodies. Failure to comply can result in the loss of authorization and ...

IFPMA, has called for greater inspection reliance between regulatory agencies to help biopharmaceutical companies reduce GMP ...

This course provides a basic understanding of current Good Manufacturing Practice (CGMP) regulations and their impact on product quality and patient safety. Good Manufacturing Practice (GMP) is a term ...

The US Food and Drug Administration (FDA) recently issued three warning letters to facilities in China, the US, and India for ...

PREFAB MODULE VENDOR: Germfree Laboratories Inc. The first large-scale prefabricated and multimodular Current Good Manufacturing Practices (cGMP) manufacturing facility built in the nation also helps ...