Sabine Paris, PhD

After graduating in pharmacy and receiving a PhD in Pharmaceutical Analytics, Sabine Paris worked in the areas of marketing authorisation for medicinal products, medical science and medical marketing for nine years.

During this time, she was a member of the medical-pharmaceutical committee of the German Association of Pharmaceutical Manufacturers (BAH) and a member of the executive board of the association for fair advertising for medicinal products INTEGRITAS.

In 2005, she joined the Central Authority of the Länder for Health Protection with regard to Medicinal Products and Medical Devices (ZLG). Her responsibilities as Head of Pharmaceutical Division at the ZLG included the cross-country quality system of the authorities responsible for the control of medicinal products, the coordination of 14 expert groups and as a national point of contact for the exchange of GMP information with European and MRA partners.

Sabine Paris was the ZLG representative for the regulatory authorities of the federal states in the European committee of the GMP/GDP Inspectors Working Group of the EMA and in the international PIC/S committee.

She is author or co-author of the following chapter of GMP Compliance Adviser:

• A.5 Nitrosamines in medicinal products: relevant in development, marketing authorisation, quality control and supervision
• 20.B Regulatory principles
• 21.B Official inspections
• B.5 International Cooperation (MRAs)