Placebo development

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

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