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EU Import Testing & QP Release

With state-of-the-art analytical laboratories we are able to provide First site of EU Import Testing services for bulk product to facilitate your product launch into the European marketplace.

We hold a Manufacturers Import Licence as required by EU legislation and employ a dedicated team of Qualified Persons (QP’s) to monitor and certify the release of drug product to the marketplace.

EU Import Testing & QP Release

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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