Greater Columbus: The Revisions to the Common Rule: The Big Takeaways

When:  Oct 26, 2017 from 11:00 AM to 05:00 PM (ET)
Associated with  ACRP Greater Columbus Chapter

The Revisions to the Common Rule: The Big Takeaways

Program Agenda:
  • 11:00 am ET & 5:00 pm ET – Webinar Replays
  • *Note: The same webinar will be played at both times.
Location: Online Webinar Replay

Registration Cost:
  • $2 for Chapter Members
  • $5 ACRP Members
  • $7 Non-Members
Program Description: The presentation will provide an overview of the changes made by the revised version of the Common Rule published in January 2017. The program will focus on the changes to the informed consent process and provide practical tips regarding what is required to effect consent. The program will also cover the treatment of bio specimens, exempt research, and IRB review. The program materials include a redline comparing the January 2017 Common Rule to the prior version.

Upon completion of this Webinar, attendees should be able to:
  • Identify the changes made to the informed consent process and the waivers of consent by the revised Common Rule
  • Describe how bio specimens are treated under the revised Common Rule
  • Identify how the new Common Rule expanded the definition of exempt research and what the exempt designation means
Contact Hour Cost:
  • FREE for Chapter Members
  • $15 ACRP Members
  • $30 Non-Members
Refund Policy: Refunds will only be processed if the event is canceled by the chapter.

Level: All audiences

Speaker, Bio-sciences attorney Carrie Hanger focuses on the needs of healthcare providers and other entities engaged in clinical and pre-clinical research. With ten years of experience representing and counseling clients, Carrie provides solutions for issues relating to regulatory and corporate compliance, risk management, professional liability, enrollment and reimbursement, and business disputes. She assists clients with issues related to clinical and pre-clinical research and drafts and negotiates clinical research related documents, including clinical trial agreements, investigator-initiated study agreements, material transfer agreements, and confidentiality agreements.

REGISTRATION REQUIREMENTS: Registration via ACRP is required in order to obtain CEUs.
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Contact

ACRP Greater Columbus Chapter
(614) 425-5845
GreaterColumbus@acrpnet.org