The Association of Clinical Research Professionals

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November 2018

Webinar: Best of ACRP 2018: Key Privacy and Security Considerations Before, During and After a Study

November 8 @ 12:00 pm - 1:00 pm EST

November 8, 2018, 12:00-1:00 pm - The session will discuss the privacy and information security concerns that can occur from the time a protocol is drafted through the completion of the study.

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Webinar: Best of ACRP 2018: Adverse Event Reporting in Medical Device Trials: Requirements from a Monitoring and Auditing Perspective

November 13 @ 12:00 pm - 1:00 pm EST

November 13, 2018, 12:00-1:00 pm - This session will cover adverse event (AE) reporting for medical device clinical trials, including the following topics: the differences between pharmaceutical and device AE reporting requirements, how to understand the AE reporting requirements for device trials based on a study protocol, and a discussion on device AE reporting requirements from a monitoring and auditing mindset.

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Webinar: Best of ACRP 2018: FDA Inspections: Understand the Process and Respond Effectively

November 14 @ 12:00 pm - 1:00 pm EST

November 14, 2018, 12:00-1:00 pm - Do you understand the process, forms and expectations following an FDA Inspection? We will review the documents exchanged during an inspection and the process followed by FDA to determine whether a warning letter will be issued.

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December 2018

Webinar: Writing for Publication in the Clinical Research Field

December 5 @ 12:00 pm - 1:00 pm EST

December 5, 2018, 12:00 pm-1:00pm – This session will overview writing for clinical research journals and is designed to empower clinical research professionals to contribute to the evidence and best practices within the industry.

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Webinar: Best of ACRP 2018: Oops, I Did It Again-How to Write a (Simple) and Effective CAPA Plan

December 6 @ 12:00 pm - 1:00 pm EST

November 28, 2018, 12:00-1:00 pm - Learn the basics of what makes a corrective and preventative action (CAPA) plan.

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