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.
23rd September | 4PM | Free
Human biological specimens are essential to biomedical research, but sourcing and using them responsibly requires careful consideration of informed consent, donor privacy, data protection and regulatory requirements.
Join BioIVT’s Compliance & Regulatory Affairs team for practical guidance on the key requirements you need to understand and how they can be applied to your research. Access the free webinar by registering for a Drug Target Review membership or logging into your account.
Why this matters:
Whether you source, purchase or work with human biospecimens, understanding your ethical and regulatory responsibilities is essential to protecting donors, maintaining compliance and supporting responsible research.
This webinar will help you navigate these considerations with practical examples and guidance from BioIVT’s Compliance & Regulatory Affairs experts.
What will you learn:
- Understand the key requirements: Explore the ethical and regulatory requirements governing the collection, sourcing and use of human biological specimens.
- Protect donor privacy and data: Learn how informed consent, privacy and data protection principles apply when working with human biospecimens and associated data.
- Manage compliance challenges: Discover practical approaches to maintaining compliance and managing deviations when requirements are not met.
- Apply best practice: Explore considerations for collecting, handling and using human biological specimens responsibly throughout the research process.
- Get your questions answered: Take part in a live Q&A and put your questions directly to BioIVT’s Compliance & Regulatory Affairs team.
Access the free webinar by registering for a Drug Target Review membership or logging into your account.
Practical guidance for working with human biospecimens
This webinar isn’t just an overview of regulations. Case studies and practical examples will demonstrate how ethical and regulatory principles can be applied in real-world research settings.
You’ll gain a clearer understanding of what responsible and compliant use of human biological specimens looks like in practice and how these considerations can be applied to your own work.
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.
Who should attend?
This webinar is relevant to scientists and research professionals who source, purchase, collect, handle or work with human biological specimens and associated data. It will also be valuable for professionals involved in compliance, regulatory affairs and responsible research practices.
Access the free webinar by registering for a Drug Target Review membership or logging into your account.
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.