Regulatory Affairs Management

Regulatory Affairs Management

Regulatory Affairs Management


Through its local presence in different countries and continuous communication with regulatory authorities, ClinServ has a strong understanding of the local requirements.


Regulatory Affairs Management services mainly include the following:


·         Mastering all local regulatory submissions (EC/IRB) in compliance with  local regulatory authorities requirements per country


·         Regulatory Consultancy & submissions


·         Clinical Trial Agreements customization and budget Negotiation


·         Registration dossier