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An Overview of the Recent SACHRP Recommendations Around Payments in Clinical Research
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Have WCG IRBs adopted the 2018 revisions to the Common Rule for the Protection of Human Subjects?
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What is the IRB’s responsibility for the review of updated Investigator Brochures?
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Is it ethical to pay subjects for referring friends to a clinical research site?
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Question: What are the signature requirements for translated informed consent documents?
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Question: Can the IRB approve reimbursement of copays for routine costs in a clinical trial?
Will an IRB allow reimbursement for co-pays for routine patient care costs associated with participation in a clinical trial when the costs are covered by insurance, but the subject is responsible for
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Challenges in Ethical Review of Research Involving Complementary and Integrative Medicine
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