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.
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