Process Validation in Pharmaceutical Industry Process validation plays a vital role in ensuring the quality, safety, and efficacy of pharmaceutical products. It is a systematic approach that… Read More

Featuring 15 above ground pool with deck ideas including the cost of constructing above-ground pool. Above ground swimming pools have been an alternative to in-ground residential pools si… Read More

21 CFR Part 11 EMEA Good Manufacturing Practices Guidelines: Annex 11 (European Union) Part 11 and Annex 11 provide detailed information on the assembly and storage of electronic data genera… Read More

http://www.manostaxx.com The purpose of this guideline is to provide design and construction suggestions for cleanrooms housing bio-pharmaceutical processes. Scope The … More Read More

Disposable medical devices, including syringes, implants, cannulas (flexible tubes) and intravenous sets, are required to be sterile. Given that plastics cannot be subjected to sterilisation… Read More

Pharmig are hosting a one day meeting on cleanrooms and contamination control:16th February 2017 – Warwickshire (Near Birmingham International Airport)Attend and receive FREE Pharmigs… Read More

As a prototype for the future, is it possible to consider an energy efficient filter system that cost-effectively maintains airflow towards a reduced rate of change? Michael Rodd, Chief Sale… Read More