We support you in implementing your research objectives as well as in case of legally required tests.
For the purpose of regulatory approval for pharmaceuticals or medicinal products we conduct studies regarding toxicity, biocompatibility and pharmacokinetics. Our institution is certified according to GLP (good laboratory practice). We offer you a detailed support prior and during the studies:
- Advice for the study design
- Assistance with legal and regulatory requirements
- Preparation of necessary documents for regulatory permissions
- Conducting an statistical evaluation of the tests
Here you'll find the GVO documentation form.
Link to the Gentechnik-Aufzeichnungsverordnung (GenTAufzV), only available in German.