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Neala Lane, MS, CCRC
Associate Director, quality Improvement Office, Indiana University
- Project Managers
- Regulatory Affairs/Compliance
- Quality Assurance
- Clinical Research Administrators
There are many steps that must be taken to assess risk and integrate quality when developing, initiating, and conducting a clinical trial. These steps are crucial for every type of clinical trial. This session will describe e how to apply those principles to investigator-initiated clinical trials utilizing tips, tools and templates available to help along the way.
4:45-5:00 Registration and Check in
6:00-6:15 Q & A
1 contact hour has been approved for through ACRP. Membership is not required for online registration/application of contact hours. Contact Hour Cost:
- $0 Chapter Members
- $15 ACRP Members
- $30 Non-Members
To receive contact hours: Purchase the contact hours, sign in at the registration desk and attend the program. Log on to the ACRP website then “My Courses” to complete the evaluation no later than 30 days following the event and obtain the online certificate. After 30 days, contact hours are no longer available.
Refund Policy: No refunds will be provided unless the chapter cancels program.