Clinical Trial Supplies and Quality Assurance

The expectation from the regulatory agencies (and volunteers and patients) is that all medicinal products intended for human (or veterinary) use will be manufactured to the level cGMP commensurate with the stage of clinical development.

In addition, scale-up will be inevitably part of any successful clinical development project. The correct integration of clinical trials supplies manufacture and scale-up can save both time and resources.

FinnBrit Consulting can advise clients on the appropriate level of GMP for the provision of clinical trials supplies including integration of scale-up.

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All information published throughout is intended for information only, and does not contain any warranties, implied or otherwise.

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