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.
Your practical toolkit for EU pharmaceutical regulatory affairs.
Calculate variation fees, estimate workload in hours and plan budgets with the Variation Toolbox. Navigate the new EU Pharma Package and explore regulatory protection periods with the EU Pharma Package Explorer. Compare authority fees across EU marketing authorisation procedures, assess parallel DCP submissions and identify cost-effective RMS options with the MA Fee Navigator.
Everything you need to make regulatory planning easier, faster and more transparent – all in one place.
Dr. Tom Deutschle
Graduate Biologist (Dipl.-Biol.), M.D.R.A.
Irma-Keilhack-Ring 20
22145 Hamburg
Germany
Mobile: 0177 2142087
info@pharmazulassung.de