Content Contributor Linda Reuter

Linda Reuter, CIP

Biomedical Research Alliance of New York (BRANY)

Linda is the IRB Director at BRANY. She holds a BS in Biology and MS in Health Science from SUNY StonyBrook, and has been a certified IRB professional since 2001. Over a 30 year career, Linda spent 20+ years in various IRB-related positions at Northwell Health, New York’s largest health care provider. As a consultant, she has traveled the country providing administrative support, IRB training and education, audit services, and general consulting to numerous IRB programs. She has provided extensive training to individuals preparing for the CIP certification exam, and has also contributed to various publications in her field.

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Informed Consent and Clinical Investigations: A Focus on the Process

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Explores current challenges and improvement strategies related to informed consent.

Informed Consent and Clinical Investigations: A Focus on the Process

Quality Improvement Activities and the Common Rule

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Learn to differentiate between QI activities and the types of activities that constitute regulated research involving human subjects.

Quality Improvement Activities and the Common Rule