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. 

 The QP can either be named on your IMP licence or on the licence of the clinical trials packaging organisation providing a seamless review and release of IMP's.

We design and manage solutions specific to your trials, or work with your existing suppliers to ensure that the supplies comply with legal requirements.

We achieve this by using dedicated professionals who work directly for you on a "time requirement" basis.  This essentially means that you have access to all the resources of DMB Consultancy but only pay for the time you use.

This is a much more cost-effective solution than using an interim or full time solution. Ensuring that new products are developed on-time, on-budget and in compliance with the latest regulatory standards.