The revised EU Annex 1 guidelines released in August 2022 recommend various practices for manufacture of sterile medicinal products in particular but the general principles can be applied in the manufacture of other pharmaceutical products too.

Our endeavour via our website is to provide ongoing inputs on current best practices and tools that can be used in manufacturing of APIs, OSDs, Injectables, etc with specific focus on Cleaning, Disinfection, Gowning and related Services depicted in the links below.

Visitors to our website are encouraged to use our “Insights” page to access articles, videos, blogs on various practical aspects of contamination control including Facility Maintenance which is an important aspect not only for contamination control but also for extending the life of the facility.
Since these topics are vast and may need customised solutions for different situations we encourage you to contact us with specific needs.