Autoren

Michel is a graduate biologist from the University of Fribourg, Switzerland.

Since 1997 he is inspector of manufacturers of dosage forms including distributors and APIs with Swissmedic, the Swiss agency for therapeutic products.

Before Michel was QA manager in a Swiss medium size pharmaceutical company, specialised in the development of galenical formulations. Michel has worked in ICH (Q7a, GMPs for APIs), is participant to the EDQM (European Department for the Quality of Medicines) inspection programme for CEP (Certification of Suitability of the European Pharmacopoeia), member of the PIC/S Executive Committee and MRA officer for the MRA between Canada and Switzerland.