About Us
IMP is managed and operated by two directors who have over 35 years of experience not only within the pharmaceutical industry but also as independent consultants to the industry. IMP offers a small scale, hands-on; audit, reporting, project management, secondary labelling and GMP storage service.
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IMP provides a dedicated point of contact to facilitate excellent communication, project updates, on time delivery all performed in accordance with industry standards and signed Quality Agreements.
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IMP is licensed to provide labelling, secondary packaging with temperature monitored and controlled storage facilities. IMP offers a real advantage for setting up your clinical trials supplies to the UK and the EU in the most efficient and cost effective way. We understand expectations of communication, delivery of service, product and provision of resources to meet our customer’s expectations. Our expertise in the requirements of the regulatory authorities can assist our customers should they have questions that extend beyond the agreed project boundaries.
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IMPs MHRA Licence number is: MIA(IMP) 46345
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