Exploring the Transformation of Registries in the 21st Century
Christina Jackson, MJ, BSN, RN, CHRC, CCRC
- 6:00 – 6:30 pm – Registration & Dinner
- 6:30 – 7:30 pm – Presentation (including Q&A and Closing)
- 7:30 – 7:45 pm – Networking
Registries are data collection tools typically used to better understand long-term trends in some certain specific population. When designed appropriately, registries can be used as a data source within which clinical trials can be performed. In recent years, the changes we have seen regarding comparative effectiveness research, the medical device industry, and now the push of utilizing “Big Data” are increasing the volume and complexity of registries we encounter in healthcare. This program will help to differentiate clinical registries and research registries and review the impact it may have in clinical trial billing.
Upon completion of this Seminar, attendees should be able to:
- Identify different types of registries.
- Apply applicable regulations to registries.
- Understand how changes within the medical device industry affected registries.
- Identify which type of registries have clinical trial billing concerns associated with them.
Target Audience: Executives, Risk Management /Quality /Safety Professionals, Principal Investigators, site managers or others engaged in clinical research
- $5 Chapter Members
- $10.00 All Others
Contact hours: 1.0 Contact hours have been applied for through ACRP.
Membership is not required for online registration of contact hours.
To receive contact hours: Purchase the contact hours, sign in at the event, and attend the program. Log on to the ACRP website then “Learning Portal” to complete the evaluation no later than 30 days following the event and obtain the online certificate.
Contact Hour Cost:
- $0 Chapter Members
- $15 ACRP Members
- $15 Non-Members
Refund Policy: There are no refunds unless the program is cancelled by the chapter before the start of the program