Clinical Research Management and Study Monitoring

Thanks to our expertise in ICHE 6, our investigators networks in both France and Middle East, and our experience in dealing with ethics committees and regulatory authorities, our well-trained staff is able to provide you with a service to cover all your needs:

 Medical Writing

ClinServ International is proud of using its long expertise in medical & regulatory writings since the set-up of the first ICH documents and guidelines, to fit your needs in:

 Quality Assurance and Consultancy

Thanks to our European expertise in auditing and training according to ICHE6 and local regulatory, as well as our location in the Middle East, our QA team is very happy to provide stand-alone QA services on the Sponsor's behalf, to support the development, maintain and management of QA system

 Clinical Data Management and Biostatistics

We work to internationally accepted ICH guidelines for Data Management and Biostatistics (ICH-E2, E3, E6 and E9) and can provide you with the following services:

 Pharmacovigilence and Regulatory Affairs

Pharmacovigilance and Regulatory Affairs.

 Marketing Support, Translation and Printing

Marketing Support, Translation, Printing, Staffing.