Pharmaceutical regulatory affairs is an exciting field that never gets boring and is constantly evolving.
My expertise in pharmaceutical regulatory affairs covers the entire product lifecycle, new marketing authorisation applications, product information texts, electronic Product Information (ePI), and much more. I would be happy to support you as a freelance consultant or as an employee.
Nobody enjoys calculating variation fees — but the Variation Toolbox makes this task much easier. It also allows you to estimate the regulatory affairs workload for variations in hours and prepare a budget plan. The Classification Guideline is integrated and easy to search:
The Legal Toolbox helps you navigate the new pharmaceutical legislation (Directive 2023/132 and Regulation 2023/131) and provides a clear overview of the new periods of regulatory protection.:
Dr. Tom Deutschle
Graduate Biologist (Dipl.-Biol.), M.D.R.A.
Irma-Keilhack-Ring 20
22145 Hamburg
Germany
Mobile: 0177 2142087
info@pharmazulassung.de