Corporate Management

Dipl. Ing. Christiane Fürstenberg

Masters of Applied Science in Food and Packaging Technology

8 years experience in research, development and implementation of the most modern methods of instrumental analysis, as well as executing these methods in the manufacturing process of a pharmaceutical supplier of natural medicines.  In charge of the microbiological lab, including monitoring of production in accordance with current GMP guidelines. 

16 years of scientific activity in Regulatory Affairs, Research and Development and Quality Assurance at a global manufacturer of medicinal products, medical devices and nutritional supplements.  In charge of creating regulatory documents as well as managing the regulatory processes. 

15 years experience with successful implemented projects from customers in management, adaptations in Quality processes as well as in Operation. Evaluation of the systems in accordance with regulatory compliance and GMP conformity in customer quality system and to the requirements from contract manufacturing.

Company

Quality Pharma Projects Gmbh

advises you in defining your objectives and jointly develops a strategy towards the implementation of

Concepts for monitoring and process optimization of pharmaceutical equipment, procedures and systems
 Technical and regulatory qualification of equipment and utilities as an essential part of the quality assurance of medicinal products and medical devices
 GMP Compliance – Reviewing quality assurance and regulatory affairs in accordance with national and international regulations

Advise on relevant regulatory issues, including creating and facilitating compliant documentation (e.g. Concept of Contamination Control Strategy)