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Quality / Regulatory / Analytical Support

We hold a Manufacturers Import License as required by EU legislation and employ a dedicated team of Qualified Persons (QPs) to monitor and certify the release of drug product.

To assist your product launch into the European market place, we offer the following services:

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Translating science to targeted patient care
Supporting the development & supply of APIs
Clinical supply; manufacturing; packaging; distribution; QP
IVR; IWR; EDC; ePRO; Biostatistics
Product Development, Commercial Manufacturing, Packaging and Support