Our collective past industry experience has been gained in big pharma, CRO and the central lab environment.
We have worked on numerous multinational trials in different phases and multiple indications.
We have past and current expertise in trial set-up and management, and in regulatory authority inspections. We recently participated in a US client's NDA FDA inspection preparation, interviews and site training. Prior to this we participated in a UK client's routine MHRA GCP inspection preparation, interviews and site training.
We maintain a large network of expert contacts and trusted collaborators.
Telephone enquiries: +44 (0) 1837 82165