As experienced ‘guides’ in the GMP mountain landscape, we help you with

  • the packaging, labelling, QP-/sponor-release and delivery of your investigational medicinal products in accordance with Regulation (EU) No. 536/2014 (Clinical Trial Regulation CTR)
  • the import and QP-release of your commercial products in accordance with EU GMP guideline Annex 21
  • the implementation of a robust QM system in accordance with the EU GMP guidelines and Regulation (EU) No. 536/2014 (Clinical Trial Regulation CTR)

In short:

  • Get to know us as the mountain guide of your tour.
  • Talk directly to decision-makers – without detours.
  • Waiting was yesterday. Acting is today.
about

Your planning with picopharma

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"Straight to your goal!"

Dr. Dirk Barth
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Our achievements

Satisfied clients say more than bold words on a website.
Here’s a selection of our recent projects — we look forward to convincing you as well.

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Contact picopharma GmbH

We look forward to a non-binding discussion with you!

Our Address

picopharma GmbH

Am Weiglfeld 24
83629 Weyarn
Phone +49 151 55 777 052

E-Mail: info@picopharma.de

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    WE HAVE A FOR HEALTH

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