Pharm Research

Pharm Research was founded by a CRA to develop professionalization of the clinical research with hospital practitioner to improve the data quality and guarantee the patient safety. Our goal is to provide quality services to both Sponsors and Investigators and achieve the project objectives. We have working to develop a dynamic network of investigators in France. We are focus to establish and maintain a high quality on working relationship based on ethics-minded physicians, experimented and volunteer physicians and staff. Choosing Pharm Research will guarantee you to involve the objectives’ study and to benefit from an administrative support and a professional framework. We identify to you the potential candidates’ investigators in your region. We make assessments according to criteria such as potential number of patients, technical equipment, availability for monitoring, experience of investigator on the disease or therapeutic area and quality of data in patient files. Before starting any trial, our staff and the investigators are trained to the GCPs but also to the modalities of clinical research, the legal aspects, the ethical issues, how identify and report a Serious Adverse Event and the relationship between the investigator and the subject like obtaining an informed consent. Each clinical study is analysed to done the better rate regarding the objective recruitment of the trial. The protocol is reviewed and prepared before the initiation of the study (POS, worksheet etc.) Our employees have a solid experience in clinical trial (Clinical Research Engineering, Master's degree in Clinical Trials, Master ‘s degree of Clinical Pharmacy, Master’s degree of Quality Assurance and Audit). We are focused on Phase I-IV clinical trials both in promotion and monitoring.