Peter has supported cGMP compliance in the pharmaceutical industry since 2013 and cGLP compliance in pre-clinical research since 2007. He specializes in verification, commissioning, and qualification activities, particularly for pharmaceutical manufacturing and API equipment. His expertise includes sterile filling, freeze drying, qualified utilities, smoke visualization, and temperature mapping. In pre-clinical research, he has managed and audited infusion and toxicology studies.
Peter Burtis
