A UL course
This course provides information on the processes commonly used to select and manage a clinical contract research organization (CRO) and other supportive contract service providers for the clinical stages of the investigational product development process. The course also covers the requirements for obtaining an appropriately completed study coordinated, at least in part, by a CRO.
- Sponsor’s responsibilities when using a CRO in clinical research
- CRO pre-selection criteria and selection techniques
- Managing CROs
Who should attend?
Professionals and experts in the pharmaceutical, biotechnology, and medical device fields