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 ...
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 ...
Good Manufacturing Practice (GMP) is a system or protocol for ensuring product safety and consistency according to quality standards. GMP is important in all manufacturing industries, though it is ...
Industries that are regulated must follow good practices to meet and maintain specific regulatory and safety standards. Different industries have different guidelines that define the good practices in ...
Quality control is of paramount importance in the drug manufacturing business. A number of times within the past decade the U.S. Food and Drug Administration has issued warnings to Lupin Ltd. for ...
Regulatory approval is a major milestone in the drug development process, but it is not the final chapter in the journey.
Residues of pharmaceutical products can enter the environment during the manufacturing process, during usage, and disposal. With the growing trend in sustainable practices, the translation of ...
Synthego has adopted Good Manufacturing Practice standards for producing customized GMP-grade synthetic guide RNA (sgRNA) at its facilities, an initiative the company said will benefit its academic ...
New solutions include customized reagents that scale from bench to clinical trials, industrialized lentiviral vector ...
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