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Speaker: Cheryle Evans
Registration Fees: This event is free to register and open to the public.
Program Description: Risk-based monitoring is the process of ensuring the quality of clinical trials by identifying, assessing, monitoring and mitigating the risks that could affect the quality or safety of a study.
Who Will Benefit from this Webinar: Clinical Research Coordinators; Clinical Research Associates; Clinical Project Managers; Clinical Operations Directors and VPs; Data managers; Programmers and anyone working in research industry.
Two (2) contact hours have been approved for through ACRP. Membership is not required for online registration/application of contact hours.
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 “ACRP Learning Portal” 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: There are no refunds unless the program is .