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Written Procedures for IRBs: What Does the New Final Guidance from FDA and OHRP Mean to You?
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Ethics in Clinical Research
Pragmatic Clinical Trials: What You Need to Know
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Gene Therapy and Genomic Editing
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Not Like Everyone Else: Unique Challenges for Small & Emerging Biopharma Companies
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Ethics in Clinical Research
Compensating Participants in Clinical Research: Current Thinking
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Ethics in Clinical Research
Gene Therapy & Immunotherapy Glossary, 2nd Edition
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Investigational Drugs Outside of Clinical Trials – Understanding Expanded Access and Right-to-Try
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Subject Recruitment Materials: Understanding the Requirements for IRB Review
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Towards Total Quality Management in Human Research Protection Programs: IRB Administrative and Reviewer Activities
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