VCRO has more than a decade experience in employing ICH GCP compliant clinical study services for IND-phase and post-marketing phase IV human research programs. IND project level from multinational, regional to local programs, VCRO all has abundant experience to contribute to the client's clinical development.
VCRO’s medical writers provide scientific and strategic service from preclinical toward clinical and ultimately to NDA. These services are delivered in a systemic, constructive and specific way to ensure successful outcomes.
VCRO provides both external GCP audits and in-house quality assurance audits for all VCRO research processes and services. Quality Assurance Unit (QAU) serves as an independent group within VCRO to help our clients meeting the international ethical and scientific standards of GCP.