Avrin provides independent contract Clinical Research Associate (CRA) services with a strong focus on site monitoring to ensure compliance, data integrity, and patient safety.
Our qualified and experienced CRAs conduct on-site and remote monitoring visits, verifying protocol adherence, regulatory compliance, and GCP standards. We proactively identify and resolve issues, ensuring trials run smoothly and efficiently. With expertise across multiple therapeutic areas, Avrin supports sponsors in maintaining high-quality oversight, mitigating risks, and ensuring successful clinical trial outcomes.