NIH Biospecimens Rule

This webinar outlines key requirements, exceptions, and compliance steps under the NIH Policy on Enhancing Security Measures for Human Biospecimens.

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About this Webinar

The NIH Policy on Enhancing Security Measures for Human Biospecimens follows a broader federal trend toward tightening physical and operational controls on sensitive personal data, especially in light of DOJ’s bulk-data rule and federal concerns about unauthorized foreign access. This webinar introduces the policy’s rationale, situates it within NIH’s existing data and research-governance framework, and outlines the safeguards NIH now expects from institutions handling human specimens. Learners will gain a grounded understanding of what the policy covers, why it emerged, and what early steps they should consider.

Release Date: April 30, 2026

Language Availability: English

Suggested Audiences: Biobank Managers, Biorepository Managers, Biosafety Officers, Compliance Officers, Embryologists, Export Compliance Officers, Export Control Attorneys, Fertility Clinics, General Counsel, Grant Administrators, HIPAA Professionals, Institutional Officials, IRB Members and Administrators, IVF Clinic Directors, Principal Investigators (PIs), Reproductive Medicine Professionals, Research Coordinators

Organizational Subscription Price: Included as part of an annual subscription to our All Access Webinar Package
Independent Learner Price: $49 per person


Webinar Content

NIH Biospecimens Rule

Presented by: Nick Weil, JD, LLM, CHPC, CIPT – Epsilon Life Sciences | Meade, Roach & Annulis

Learning Objectives:

  • Understand the scope, definitions, and narrow exceptions of the NIH Biospecimen Rule.
  • Identify key documentation requirements of the NIH Biospecimen Rule.
  • Apply requirements to create compliance steps.

Recommended Use: Required
ID (Language): 22270 (English)


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