Services

Protocol Development / Case Report Form Design

GRS is able to provide complete protocol development. The final protocol will serve as the roadmap to our Client's success. GRS draws on its 20 years of experience in designing and conducting complex clinical trails in order to produce a quality protocol that meets study objectives and regulatory compliance.

GRS also designs case report form (CRF) pages in either paper-based or eCRF format. We develop our CRFs from a data management, biostatistics, project management, monitoring, regulatory, and medical perspective in order to optimize the study conduct and ensure that all CRFs conform to worldwide regulations and guidelines including the FDA, EMEA and SFDA. We shorten development timelines as well as time to study start up by offering access to a library of standardized CRF pages, experienced professionals in clinical research, and comprehensive review that result in efficient CRF development for effective study conduct.