This webinar will detail efficiencies crucial to the management of local lab data and normal reference ranges. Topics for discussion include, but are not limited to: CRF design considerations, collection of local lab ranges, cleaning the local lab data and ranges collected, programming considerations, as well as quality control.
The amount of lab data collected, and the procedures used can vary greatly depending on the clinical trial. Even the largest challenge can be overcome with well documented procedures for each step of the process.
By attending this course, attendees will learn:
- Items to consider when designing an electronic CRF to collect local lab data
- How to collect the local lab normal ranges, and manage them throughout the longevity of the clinical trial
- What to do with the local lab ranges once they are collected, loading them directly into EDC, or maintaining a separate lab database
- Methods of cleaning the local data and the normal reference ranges collected
Participants are eligible to receive CEUs upon attendance and successful completion of a web-based assessment within 30 days after the webinar. CEUs are not granted after the 30-day assesment deadline.
*Please note that a group should be constituted of max. 10 people who will be allowed to take the assessment questions after the webinar. Different members of one group will be able to log in from different regions of the world.