As a clinical research site, we offer a range of services to support the conduct of high-quality, ethical clinical research studies.
Our services include:
- Protocol development: We work with researchers and sponsors to design clinical research studies that are scientifically rigorous and ethically sound.
- Subject recruitment: We have a robust process for recruiting study participants who meet the inclusion criteria for the studies we conduct.
- Data management: We have a team of trained professionals who are responsible for collecting, managing, and analyzing data from our clinical studies.
- Site management: Our team is responsible for overseeing all aspects of the conduct of a clinical study at our site, including coordinating with the sponsor and investigator, managing study documents, and ensuring that all study activities are conducted in compliance with relevant regulations and guidelines.
- Regulatory support: We assist researchers and sponsors with the regulatory aspects of clinical research, including submitting study documents to institutional review boards and other regulatory authorities, and ensuring compliance with all relevant regulations and guidelines.
If you are a researcher or sponsor interested in conducting a clinical study at our site, we invite you to contact us to learn more about our services and how we can support your research.