Broad-ranging therapeutic expertise

IMP, Medical Devices and IMP-Device Combi

You know your product(s), we know the regulatory landscape and can assist you throughout the lifecycle of your project, from protocol development, regulatory/ethics submissions through, to data management and end of study closure/publications. We want to work with you to ensure the success of your study, as we understand that patients ultimately benefit from your innovations and interventions. We support both drug and device studies.

CRO therapeutic expertise you can rely on

We have also conducted studies in other therapeutics areas:


Studies conducted to July 2024

We have demonstrated experience in delivering across all phases of clinical trials (Investigational Medicinal Products),  with a large emphasis on early phase studies. Our medical device work includes clinical investigations pre and post UKCA/EUCE marking (Class I-III).

"The team at PHARMExcel is a pleasure to work with and deeply impressive with their depth of knowledge, competence and ability to deliver."


Need help with your study?

We know that successful partnerships can only be advanced where there is a true understanding of requirements and expectations. PHARMExcel welcome the opportunity to learn more about your specific needs so we can best determine the right delivery approach for you.