Manufacturing of clinical trial material for phase I to III can be offered either as part of the development program or as a standalone service for all dosage forms.
Our manufacturing services (according to compliance with GMP/GCP guidelines) include:
- Manufacturing of IMPs (solid dosage forms, semi-solid dosage forms and liquids) and matching placebos
- De-blistering and de-packaging of pharmaceutical products
- Blinding/manufacturing of capsules