IRB Information for Sponsors
IRB General Contact Information
420 S. Fifth Avenue
Doctor's Office Building, Suite 1010
West Reading, PA 19611
Chair: Gregory Mokrynski, MD, CIP
Director, Human Subjects Protection: Sharon House, RN, CIP
Administrative Assistant: Kathryn Nester
Reading Hospital Institutional Review Board
Reading Hospital IRB is registered and has federal-wide assurance.
- IRB Registration: IRB00002156
- FWA Number: FWA00003110
- FWA Expiration: March 11, 2020
Full Board / New Protocol
These meetings are scheduled to take place on the second Tuesday of every month The submission deadline for items to be reviewed by the Full Board is the second Monday of the month, prior to the meeting. Changes requested by the IRB must be made before the item will be placed on the final agenda.
The turnaround time is typically 30 days from submission to completion of correspondence, provided any necessary corrections are received in a timely manner.
There are non-refundable fees depending on the service being provided and proof of invoice must be provided with the submission.
Study Start-Up: Non-refundable start-up fee of $2,500 is due at the time of submission
Continuing Review: No more than $1,000 per review will be charged based on the following:
- Annual reviews – $1,000 per review
- Six-month review – $500 per review
- Less than six months – $250 per review
Amendments: No more than $500 per amendment will be charged based on the following:
- Changes to the protocol, informed consent, and other documents – $500
- Administrative changes to the protocol – $250
- Changes to informed consent, patient education or recruitment materials – $250
Exceptions: The IRB does not invoice for the following:
- Research protocols sponsored by non-profit agencies (AHA, ACS)
- Research protocols sponsored by the Federal government (NIH, FDA, DHHS)
- Research protocols sponsored by National Cooperative Groups (ECOG, GOG, NSABP, RTOG, etc.)
Any regulatory questions can be directed to the Clinical Trials Office at 484-628-8585.