Content
1 module
Rating
Course length
15 mins
Instructor
Miranda Schramm
Description
During a clinical trial, the management of the investigational product (IP) is an important task that requires great care and attention to detail. Correct IP management minimizes the risk to study participants and protects the integrity of clinical trial data.
This course aims to cover the practical concerns of IP management in the areas of accountability, storage, and administration.
Objectives
By the end of this course, you will be able to:
- Define what an investigational product is and how to find information on its use in a study.
- Determine appropriate storage, access, and record keeping for investigational products.
- Create administrative practices for the proper handling, return, and disposal of investigational products.
Certificate
By completing/passing this course, you will attain the certificate Advarra Completion Certificate
1.
RRT 232: CRC - Investigational Product Management
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