Clinical Trial Audit and Monitoring Services - Overview

Clinical trial audits and monitoring guarantee that the trial data is accurate, complete, verifiable, and in agreement with ethical and scientific norms. The quality of clinical trial monitoring is the basis for efficient execution, and the success of each clinical trial depends on it. Robust clinical trial monitoring is vital to protect the integrity of the scientific data and yield valid Regulatory data. To ensure that clinical data adhere to the protocols and international guidelines, organizations must opt for a clinical trial audit expert who is well-versed in clinical trial monitoring and auditing.

Freyr has a skilled clinical trial audit and monitoring team that showcases innovative problem-solving talents while monitoring everything from straightforward, 2-way, cross-over Bioequivalence (BE) and Bioavailability (BA) study services to large, complex, steady-state BE and BA study services. Freyr also provides independent clinical trial monitoring and auditing services for clinical and bio-analytical phases of the BE and BA studies through its highly qualified and experienced clinical monitoring team.

Our clinical trial monitoring services assist in quality control to maintain the integrity of the clinical trial per specific standards like ICH Good Clinical Practice (GCP), the United States Food and Drug Administration (US FDA), Europe, Middle East, and Africa (EMEA), the National Health Surveillance Agency or ANVISA (Agência Nacional de Vigilância Sanitária) regulations, etc.

To provide continued clinical trial monitoring, our clinical experts guide in preparing and reviewing clinical Standard Operation Procedures (SOPs). Freyr’s proactive research-site approach helps you access the best sites following a thorough audit of feasibility and analysis of the CRO/study site, along with high-quality monitoring throughout the trial duration, to ensure compliance with the applicable regulations and guidelines.