Navigating Ethical and Regulatory Requirements in Human Biospecimen Collection and Use

Navigating requirements for the use of human biological specimens in research is complex, but essential for ensuring data integrity, ethical sourcing, and global readiness. A number of BioIVT's experts from compliance and regulatory affairs recently presented on the major elements you need to be aware of as well as how they tackle challenges like audit readiness, privacy compliance, and quality oversight. Amanshe Slaney, BioIVT's Sr. Dir. of Compliance & Regulatory Affairs and DPO, provides us with the key points from this important discussion.