Whether you source, purchase or work with human biospecimens, understanding today’s ethical and regulatory expectations is essential. Join this webinar to explore informed consent, privacy and the principles that support responsible research.
Human biological specimens (HBS) are invaluable to biomedical research, but their use comes with important ethical and regulatory responsibilities. Understanding how to meet these requirements is essential for protecting donors, maintaining compliance and supporting responsible research.
In this webinar, BioIVT’s Compliance & Regulatory Affairs (C&RA) team will explain why these requirements matter, outline the key regulations and discuss practical considerations for working with human biospecimens and associated data.
What you’ll learn:
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Understand the ethical and regulatory requirements governing the use of human biospecimens
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Learn how informed consent, privacy and data protection support responsible research
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Explore practical approaches to maintaining compliance and managing deviations
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Discover the best practices for collecting, handling and using human biospecimens and associated data
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Ask BioIVT’s Compliance & Regulatory Affairs team your questions during the live Q&A
Case studies and practical examples will illustrate how these principles are applied, helping participants better understand regulatory expectations and best practice.
By the end of the webinar, you will have a clearer understanding of the ethical and regulatory requirements surrounding human biospecimens and how to apply them in their own research. The session will conclude with a live Q&A, providing the opportunity to discuss questions and challenges directly with BioIVT’s Compliance & Regulatory Affairs team.
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Amanshe Slaney – Senior Director, Compliance & Regulatory Affairs, DPO, BioIVT
Amanshe Slaney is Senior Director of Compliance and Regulatory Affairs and Data Protection Officer at BioIVT. Before joining the company, she oversaw regulatory activities for more than 30 industry-sponsored clinical trials at a large pulmonary clinic in Orlando. She holds a Bachelor of Science in Business Administration (Health Services Management), a Master of Public Administration in Healthcare Management and a Graduate Certificate in Human Resources Management from DeVry University and Keller Graduate School of Management. She has led BioIVT’s Compliance & Regulatory Affairs team for the past 12 years.
BioIVT’s C&RA Team
Amanshe will be joined by members of BioIVT’s Compliance & Regulatory Affairs team, who bring decades of combined industry experience and will share practical perspectives on the ethical and regulatory use of human biospecimens.
Is the panel discussion free?
Yes – there is no charge to watch the panel discussion, either live or on-demand.
When will the panel discussion take place?
The webinar will be taking place on 23rd September 2026.
Can I watch it later?
The panel discussion will become available to watch on-demand shortly after the live webinar takes place.
What are the benefits of attending live?
You’ll be able to ask the speakers your questions, which will be answered live in the Q&A towards the end of the session.
How long will the panel discussion be?
This panel discussion will last up to an hour.
What do I need to watch this panel discussion?
All you need is a computer with an internet connection. We recommend using headphones if possible if you’re in an office environment.