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Webinar: (06-2023) Ongoing Study Oversight: Ensuring Protocol Compliance through Postapproval Monitoring

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Description


The challenges of providing ongoing study oversight to animal and human research protocols have continually increased because of such developments as increasing complexity of the research, institutional and public pressures, and changing regulations. What has not changed, however, is the institution responsibility to maintain oversight through its IACUC and HRPP.

Implementing a postapproval monitoring program can fill the compliance gap while also serving as a pathway for providing ongoing education and for forging stronger relationships with researchers.

This webinar will address different models for providing ongoing study oversight through a postapproval monitoring program and how to use PAM visit results as part of an ongoing programmatic evaluation. Time will be reserved for questions.

What will I learn to do?
  • Articulate the principles on which PAM is founded and identify objectives of a robust PAM program.
  • Describe different models of conducting PAM.
  • Identify approaches to deciding who and what to monitor.
  • Report PAM results to key stakeholders, including oversight committees.
  • Consider how PAM results can be used when evaluating the overall animal care and use program or human research protection program
Continuing Education
Course participants who hold the Certified Professional in IACUC Administration (CPIA®) credential may apply 1.25 continuing education credits towards CPIA recertification credit for each course in the IACUC Core Training. Learn More

Discounts available for groups of various sizes from a single institution!

  • Buy 4 get 1 free
  • Buy 12 get 6 free

To receive complimentary registrations, first register the paid registrants (e.g. if you’re using the buy 4 get 1 free discount, register the 4 paid individuals first) and then email onlinelearning@primr.org with a list of those paid individuals, as well as the name(s) and emails of those to receive complimentary registration.

Group discount requests must be received at least 24 hours before the event broadcast begins. Refunds or retroactive discounts are not available.

Access Interval
Access to live content will be available for 90 days after the recording is made available. After 90 days, access to the content will be removed, but users will retain access to any certificates of attendance earned. To earn a certificate, one must complete all required sections and complete the certificate section within the 90-day access period. After access has expired, users can purchase an additional 90 days of access.

If you prefer, you can find a paper registration form here. Please send the completed form to registration@primr.org.

*Please note that you cannot purchase this webinar on behalf of others. If you would like to register a colleague or a group, please fill out the paper form or contact onlinelearning@primr.org for an invoice.

Contributors

  • John R. Baumann, PhD

    John R. Baumann is the associate vice president for research compliance at Indiana University, including the Bloomington and Indianapolis campuses, as well as the five regional campuses and affiliated hospitals. He earned his PhD in sociology from the Graduate Center of the City University of New York. In addition to his position at Indiana University, Dr. Baumann serves as a site visitor for AAHRPP, Inc., has just finished a six-year term on its Council of Accreditation and chairs the social-behavioral IRBs of the National Development and Research Institutes and the American Academy of Family Physicians. Prior to joining Indiana University, Dr. Baumann was vice provost for research at the University of Missouri-Kansas City and, before that, deputy executive director of the National Development and Research Institutes, a private, not-for-profit behavioral science research institute in New York, NY, with a primary focus on substance abuse, HIV/AIDS, and related social problems.

  • Michelle C. Stickler, DEd, CIP

    Michelle Stickler is Assistant Vice President for Research Support and Compliance at The University of Texas at Austin. In this capacity she oversees administrative operations supporting the IIRB, IACUC, IBC, Conflict of Interest, and Responsible Conduct of Research. Prior to joining UT Austin, Michelle served as Executive Director, Office of Research Subject Protection at Virginia Commonwealth University and as Associate Director for The Pennsylvania State University’s Office of Research Protections. She currently serves as a site visitor for The Association for Accreditation of Human Research Protection Programs (AAHRPP). Michelle has been involved in several NSF funded research projects focusing on ethics education and projects sponsored by the Council of Graduate Schools to foster ethical knowledge and behavior. Michelle holds a Doctor of Education in Adult Education from Penn State and is a Certified IRB Professional.

June 22, 2023
Thu 1:00 PM EDT

Duration 1H 15M

This live web event has ended.

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