Our Investigators undergo in-house, GCP, NIH, FDA Guidance for Industry – Investigator Responsibilities – Protecting the rights, safety, and welfare of study subjects training as part of their commitment to being informed about their responsibilities as Investigators.
We also provide you with a Quality Consultant to ensure that our studies are implemented and monitored according to industry standards. Continuous in-house monitoring and quality oversight takes place during all study activity. If you would like to learn more about how Vida Clinical Research could assist you or if you require additional sites for your clinical studies, please do not hesitate to contact our office.
