Post-Authorisation Safety Studies (PASS)
We turn out to be trial best recruiters at European and international level, often competing with world leading players.
Hippocrates Research has proven experience in managing operative and scientific issues of trials implying “first in man” new chemical entities.
Clinical Trials with General Practitioners (GPs)
We feature a network of 400 General Practitioners with experience in interventional regulatory and non-regulatory observational and epidemiologic trials.
Creation and Management of Registries
HR has contributed to the creation and management of a number of National Registers for patients with IBD, Lacrimal Dysfunction, Glaucoma, Migraine, Thromboembolism and more.
Medical Device Development
Over the years we have been contributing to the Regulatory system with the clinical development of Medical Devices of all classes under European Directive no. 2007/47/EC.
Hippocrates Research is accredited by EudraVigilance as a service provider for ICRSS data collection, medical reviews, literature reviews, global services, training, etc.
a broader definition of services includes communication, regulatory, and archiving competences which have been developed with Partners playing leading roles in their fields.
Integrated Marketing Support
We manage press conferences, observational and spontaneous trials, CME events, we draw up information material and brochures in support of product.
Long Term Archiving
Hippocrates Research is Leader in Europe in the Long Term Archiving of documents produced by clinical sites related to trials.
Hearings with Regulatory Authorities
Hippocrates Research promotes and manages hearings and assists the Sponsor in hearings with Regulatory Authorities.