Mawdsleys can provide a complete clinical trial product supply service to pharmaceutical companies, hospitals and CROs which helps satisfy patient needs and deliver clinical trials on budget. As well as the supply of clinical trial drugs, we can help with the fulfilment of clinical trial regulatory requirements. Those who partner with us can be confident in the high service levels they will receive.
Whatever the requirements or time constraints, we have the experience to support pharmaceutical companies, hospitals and CRO's. We can source all clinical trial supplies (IMPs, ATMPs, biologics, comparators, placebos), import clinical trial products, and manage QP Release certification and storage and distribution (including cold chain).
We have extensive expertise in pharmaceutical procurement and logistics, are specialists in clinical trial regulations and have strong relationships with Competent Authorities.
To support our clients further, we offer a range of clinical trial manufacturing services which all conform to cGMP:
As part of Mawdsleys, the clinical trial division offers high quality services designed to support the delivery of clinical trials on time and on budget, with the patients always in mind.
Clients will benefit from the high service levels we pride ourselves on always delivering. Many of our clients come through to us on recommendation. Our friendly team of EU Qualified Persons (QPs), Pharmacists and Clinical Trial Specialists work together to help our clients, understanding the time and budget pressures they face on a daily basis.
Mawdsleys can provide the following clinical trial services:
Helping ensure patients have access to the drugs they need, when they need them.
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