The clinical trial audit and monitoring is accurate, complete, verifiable, and in agreement with the ethical and scientific norms to protect the integrity of the scientific data. The quality of clinical trial monitoring is basis for efficient execution, and the success of clinical trial. Robust clinical trial monitoring is vital, as it yield valid Regulatory data adhering to the protocols.

Revive provides qualified innovative clinical trial audit and monitoring team that showcases problem-solving study services for both the clinical and bio-analytical phases of the bioequivalence (BE), and bioavailability (BA) studies.

To provide continued clinical data monitoring, our experts also guide in preparing and reviewing clinical Standard Operation Procedure (SOP). Revive’s proactive research site are audit of feasibility and analysis of the CRO/study site to ensure compliance with the applicable regulations and guidelines.

Our clinical monitoring services overlook quality control during clinical trials to maintain the integrity of the trial as per specific standards like ICH (GCP), (USFDA), (EMEA), ANVISA regulations, and so on.