Clinical Operations and Patient Affairs
We support clinical research with efficient trial management, sample collection, and workflow optimization. By combining well-equipped laboratory with clinical expertise, we enhance patient recruitment, compliance, and efficiency, accelerating the development of new therapies.
Clinical Trial Administration
Our services include IRB application and ethical approval, protocol development, regulatory submissions, and site selection and monitoring. We also provide expert consultancy for trial design, regulatory strategy, and compliance with GCP guidelines. From data management to adverse event reporting, we handle all aspects of clinical trial oversight, ensuring your trials run efficiently, meet regulatory standards, and deliver high-quality data for drug and device development.
Please contact us for consultation and further details.