Management of Observational Studies

Our team is an expert in the requirements of relevant authorities in the context of clinical and analytical research, and provides comprehensive information on legal requirements, application processes and approval schedules specific to each country. It supports the timely and complete completion of applications by providing a complete list of all required documents from the very beginning of the process.

VİTAL CRO Consulting provides comprehensive support to sponsors in providing the necessary translations, preparing application files and meeting all regulatory requirements in the best way, starting from the contract phase. It provides guidance in all stages of clinical and analytical research, including the following services:

• Preparation of application files in accordance with regulations

Determination and implementation of country-specific legal requirements

Provision of necessary translation services

Follow-up and timely completion of application processes

Contract management and execution of official procedures

Our experienced team offers the best solutions to ensure that research progresses quickly, reliably and within the framework of legal compliance.