Validation of Cleaning Programs is now a mandatory requirement under most GFSI food safety standards. Luckily, Safefood 360° has compiled everything you need to know to keep your external auditors more than happy.
Validation is a broad concept in the pharmaceutical manufacturing industry. It includes process validation, analytical method validation, equipment validation, cleaning validation and system validation.
The DMC session, had been organized by the Pharmaceutical Industry Committee headed by Dr. Mohamed Esmat, and held at the Faculty of Pharmacy, Cairo University, ended on Saturday with a total of 84 trainees from around the country.
Bacteria could be programmed to efficiently produce drugs, thanks to breakthrough research into synthetic biology using engineering principles, from the University of Warwick and the University of Surrey.
Regulatory authorities act as a guardian that ensures the safety, efficacy and quality of drugs available to the public, to identify the strengths and weaknesses of drug regulation and to propose strategies to improve drug regulation.