Content Contributor Linda Reuter

Linda Reuter, MS, CIP

Biomedical Research Alliance of New York (BRANY)

Linda Reuter has been involved with IRB Administration in various capacities for over 30 years, currently serving as the Sr. Director for BRANY IRB. Responsibilities include supervising the IRB staff, maintaining compliance with the IRB SOPs and applicable regulations, supervising pre and post-IRB meeting activities, expedited reviews, continuing reviews, protocol monitoring, continuing education, development of strategic goals for the organization, maintaining AAHRPP accreditation standards, policy maintenance and development, and training/mentoring of IRB staff. Linda formed IRB Consulting, LLC in 2012, providing IRB administrative services, training and education, audit services, and general consulting to numerous IRB programs across the country.

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Informed Consent and Clinical Investigations: A Focus on the Process Informed Consent and Clinical Investigations: A Focus on the Process
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Series: Webinars

Explores current challenges and improvement strategies related to informed consent.

Doctor and Woman discussing consent
Quality Improvement Activities and the Common Rule Quality Improvement Activities and the Common Rule
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Series: Webinars

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

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On Research Podcast: Consent in Research On Research Podcast: Consent in Research
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Season 1 - Episode 7
Informed consent applies to research in the social-behavioral, physical, and medical sciences.

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On Research Podcast: Consent in Clinical Research On Research Podcast: Consent in Clinical Research
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Season 1 - Episode 8
Voluntary informed consent safeguards participants from potential research-related harm.

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