Bryan O’Donnell, Head of Quality at Gaelic Laboratories, explains how to navigate GMP challenges to ensure your company ...

The Union ministry of health and family welfare has issued the final notification extending the deadline for implementation of the revised Schedule M manufacturing standards to one more year for the ...

The "Mastering Pharmaceutical Document Management: Strategies for Compliance and Efficiency" training has been added to ResearchAndMarkets.com's offering. This specialized course offers a deep dive ...

The pharmaceutical industry is highly regulated and maintains strict standards of precision. Embracing automation and the advanced digital tools conceived through the principles of Pharma 4.0 aim to ...

The comprehensive program is not only a quality management system audit, but also a process certification program ... Assurance process certification program, customers receive a GMP certificate and ...

More audits will follow. The contract between the sheriff and ANF Group included what’s known as a Guaranteed Maximum Price (GMP), a limit on the amount the owner pays a contractor for ...

This form serves as a declaration of intent from manufacturers, detailing how they plan to meet the Good Manufacturing Practices (GMP) and equipment requirements ... including potential factory ...

The Stability Program is being conducted in collaboration with HYTN’s GMP-licensed laboratory partner. Upon successful completion, HYTN expects to provide an initial six-month stability statement for ...

From this assessment, an Audit Plan is developed and presented to the Audit Committee for approval. The plan addresses high-risk areas as well as allocates time for special ad-hoc projects. In ...

If you own a U.S. trademark registration, you have likely encountered (or will encounter) an audit by the US Patent and ...