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 We have many years experience in the manufacturing, labelling, storage and distribution of Investigational Medicinal Products for clinical trials worldwide.
We offer comprehensives services in support of clinical trials for both the public and private sector: Management of the Manufacture and Release of Clinical Trial Supplies ensuring that your Investigational Medicinal Products (IMP's) are manufactured on-time, cost effectively and in compliance with EU Directives, Good Clinical Practice (GCP) and Good Manufacturing Practice(GMP)
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IMP Importation into the EU |
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We are able to provide Qualified Person (QP) release of Investigational Medicinal Products (IMP's) and help with the release of Active Pharmaceutical Ingredients (API's) We can also offer contract Qualified Person services to cover temporary or long-term requirements. |
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Clinical Packaging, Storage and Distribution |
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DMB Consultancy can help manage all aspects of your requirements for clinical trial packaging, storage and distribution.
We have excellent knowledge of the service providers within the UK and the USA and design and assist with all aspects of the process.
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DMB Consultancy can also assist with sourcing of comparator products globally with procurement from a variety of sources both from both within and outside the EU, ensuring you get the best possible price with short lead times and consistant service levels.
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We can provide a wide variety of services for the manufacture of Clinical trial materials, including the sourcing and manufacture of placebo products. We have excellent knowledge about the current market situations and the providers of different dosage forms and their capabilities. |
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