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 ...

Good Manufacturing Practice (GMP) compliance in biologics contract manufacturing underpins product safety, efficacy, and ...

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 ...

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 ...

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 ...

New solutions include customized reagents that scale from bench to clinical trials, industrialized lentiviral vector ...

Our Cell Processing Facility (CPF) is a Good Manufacturing Practice, or GMP, bioprocessing manufacturing facility that supports the reproducible production of human hematopoietic or immune-competent ...

The contract manufacturing organization agreed to purchase the American biotech's good manufacturing practice production ...