Meeting ethical & regulatory requirements when using human biological specimens

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.

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.