Diapharm expands its Regulatory Affairs division: Petra Kist and Dr Stefanie Zumdick join the team

Pharmaceutical service provider Diapharm (www.diapharm.com) has expanded its Regulatory Affairs team this September with the addition of Petra Kist and Dr Stefanie Zumdick. Some of the duties performed by the new members will be to help support manufacturers of medicinal products and food supplements with the registration, testing and approval of their products.

Petra Kist is joining Diapharm’s Oldenburg office from G. Pohl-Boskamp GmbH & Co. KG, where she was Head of the Approvals Department. The specialist Drug Information Pharmacist will from now on be responsible for national and international drug approvals and the creation of the corresponding dossiers. Petra Kist studied pharmacy at the University of Kiel, followed by a Master’s degree in Drug Regulatory Affairs from the DGRA in Bonn.

Dr Stefanie Zumdick is joining Diapharm’s Regulatory Affairs team for food supplements in Münster. The nutritional chemist has been Head of the Department for Cereal-based Foods at the Chemical and Veterinary Investigation Office (Chemisches und Veterinäruntersuchungsamt, CVUA) for Münsterland-Emscher-Lippe, and most recently worked in the Department for Cosmetics and Commodities at the CVUA Ostwestfalen-Lippe in Detmold. At Diapharm, she will support manufacturers of food supplements in product design, applications for health claims, and borderline issues. Dr Stefanie Zumdick studied in Münster, where she obtained her PhD at the Institute for Pharmaceutical Biology and Phytochemistry.

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