Key market opportunities include identifying emerging trends and innovations, leveraging insights from recent mergers and acquisitions, optimizing supplier selection, staying informed about regulatory ...

The "How to Interview During GMP (Good Manufacturing Practice) Audits Training Course (Mar 12, 2026)" training has been added to ResearchAndMarkets.com's offering. Ensuring compliance with Good ...

Low compliance by the country’s 8,500 small and medium enterprises (MSMEs) manufacturing pharmaceuticals would raise the risk ...

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 ...

The Union Health Ministry is holding discussions with state governments and drug regulatory authorities to consider granting ...

The course covers the need for and history of Pharmaceutical GMP as well as the key GMP requirements at the various parts of a pharmaceutical manufacturing site, from goods-in to despatch of the ...

Process development is the exercise of creating new and improved manufacturing methods, optimizing them in terms of time and financial efficiency while maintaining regulatory compliance and product ...

The Union Health Ministry is in talks with states about extending the deadline for pharmaceutical companies to meet new ...

Notified in December 2023, the revised Schedule M has shifted the focus from “good manufacturing practices” to “good ...

A generous donation from a pioneer in pharmaceutical and biotechnology manufacturing will establish the William D. Young Institute for Advanced Manufacturing of Pharmaceuticals at Purdue University.

The health ministry is unlikely to extend the Schedule M deadline for MSME pharma firms beyond December 31, 2025, as it ...

In an exchange filing, the company said the current Good Manufacturing Practices (cGMP) inspection was conducted by the US ...