We offer both on-site and remote monitoring services tailored to the specific needs of your study, ensuring flexibility and cost-efficiency.
We offer both on-site clinical monitoring and remote monitoring services, tailored to the specific needs of your study, ensuring flexibility and cost-efficiency.
Our monitors implement risk-based monitoring in clinical trials, focusing on high-risk areas of a study, optimizing resources while maintaining data quality.
Micron offers oversight of all services employed in the development of your product, including other CROs.
With in-depth knowledge of ICH-GCP guidelines and evolving global regulatory requirements, our team ensures end-to-end regulatory compliance in clinical trials. We are adept at gaining the speediest approval from health authorities for your study to proceed.
Patient safety and data integrity are our highest priority. We ensure your trial meets the strictest standards for patient risk mitigation while safeguarding clinical data accuracy and regulatory readiness for submission.
Our clinical research professionals have expertise across multiple therapeutic areas, ensuring that monitoring is conducted with a full understanding of the clinical and scientific context. Our focus is primarily infectious diseases, oncology and immunology, but we have also worked in many other areas.
109B Lancaster Way Business Park
CB6 3NX, Ely, Cambridgeshire
England, United Kingdom
12022 Blue Valley Parkway, Overland Park
Kansas 66213, United States of America
5 Regency Drive, Building C, Route 21 Corporate Park Irene, South Africa
Harju maakond, Tallinn, Kesklinna linnaosa
Viru väljak 2, Tallinn 10111, Estonia
9 Regency Drive, Building B, Route 21 Corporate Park
Irene, 0157, South Africa