Astrid Stockrahm-Uhling

Internal Advisor for GMP Compliance

DFE Pharma


Astrid graduated in Chemical Engineering and initially worked for a Contract Research Organisation in execution of Phase I and II Clinical Trials. She then joined JANSSEN-CILAG in 1995, spending 6 years as Clinical Research Manager and another 5 years in Quality Assurance. 2007 she joined DFE Pharma and took up the position as QA Manager with overall responsibility for QA and Regulatory activities worldwide. Since 2014 she is Internal Advisor for GMP compliance and the company’s official representative in IPEC activities. Astrid led the IPEC Europe task force Revision of Quality Agreement Guide, and is now leading the GMP Guide revision team.

« Back