Med/Sci
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Ethics in Clinical Research
Compensating Research Participants FAQ
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AIMS User Guide
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Ethics in Clinical Research
Ask the Experts: When Do I Report a Protocol Deviation to the IRB? Do I Need To Report a Summary of Deviations at the Time of Continuing Review?
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FDA & ICH
What documentation needs to be submitted to the IRB for an IND exemption request?
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Cell & Gene Therapy
[Video] Institutional Biosafety Committee Review: Strategies to Secure Rapid IBC Approval for Human Gene Transfer Trials
Videos![](https://www.wcgclinical.com/wp-content/uploads/2021/04/8f4497f9a3d1b4f9d8c5c537f00d7041.jpg)
IBC Review: Strategies to Secure Rapid IBC Approval for Human Gene Transfer Trials
Videos![Two colleagues submit their study for IRB review on WCG IRB Connexus, streamlining their protocol review.](https://www.wcgclinical.com/wp-content/uploads/2023/02/banner-collaboration-desk-masks-e1685734978696.jpg)
Clinical Endpoints
See How WCG Helped a Mid-tier Biopharma Respond to an Urgent FDA Request, and Adjudicated 400 Endpoints in Just a Few Short Weeks
Case Studies![](https://www.wcgclinical.com/wp-content/uploads/2021/04/medical-record-digital.jpg)
Ethics in Clinical Research
Does research involving retrospective review of patient charts require IRB review?
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Ethics in Clinical Research
The IRB’s Perspective: Determining Optimal Compensation for Clinical Trial Participants
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COVID-19