2nd Annual Extractables & Leachables 2026 Webinar

Place: Online

Date: April 2026
Language: English

Key poins:

  1. Updates on Extractables and Leachables Regulations and Testing
  2. Discussions on Best Practices for Risk Assessment
  3. Strategies for Navigating Regulatory Complexities
  4. Advanced Analytical Techniques for E&L Studies
  5. Ensuring Patient Safety through Material Compatibility Assessments
  6. Exploring the Impact of Emerging Technologies on E&L Analysis
  7. Implementing Quality Assurance Practices to Ensure Compliance and Reliability in E&L Testing
  8. Enhancing Manufacturing Processes to Minimize Extractables and Leachables and Ensure Product Safety
  9. Challenges with Novel Materials in E&L Testing

Welcome to the 2nd Annual Extractables & Leachables 2026 Conference!


This two-day event brings together industry leaders, regulatory experts, and stakeholders from both the pharmaceutical and medical device sectors to explore the latest developments in E&L testing and regulation.

Gain insights into emerging trends, best practices, and innovative approaches for evaluating chemical safety in drugs, devices, and combination products. Connect with experts, share knowledge, and stay ahead in this critical area of regulatory compliance and material safety.

Do not miss the opportunity to advance your expertise, network with peers, and discover solutions that drive safety and innovation.

The conference contains

10+ expert-led sessions

Q&A Sessions

Panel discussion

Post-webinar materials

Certificate of Attendance

Keynote Sponsors

Our Past Speakers:

Event Sponsor

Benefits of attendance:

  • Meet new connections in groups or one-on-one.
  • Strengthen your professional network.
  • Gain cutting-edge insights from industry experts.
  • Stay up to date with the latest regulatory changes.
  • Enhance your knowledge and professional development.
  • Enjoy an engaging and informative online experience!

Media Partners

Who should attend:

The Extractables & Leachables in Medical Devices 2025 Conference is tailored for professionals across the medical device and pharmaceutical industries who seek to enhance their understanding of E&L regulatory compliance and safety practices:

  1. Regulatory Affairs Professionals: Responsible for ensuring compliance with E&L regulations and standards.
  2. Medical Device Manufacturers and Suppliers: Engaged in the production and distribution of medical devices and drug packaging systems.
  3. Quality Assurance and Quality Control Personnel: Tasked with maintaining product safety, regulatory compliance, and reliability.
  4. Toxicologists and Risk Assessors: Evaluating potential health risks associated with extractables and leachables in both medical devices and pharmaceutical products.
  5. Analytical Scientists: Conducting E&L studies using advanced testing methodologies to assess material safety.
  6. Material Scientists and Engineers: Assessing material compatibility and safety for medical devices and drug delivery systems.
  7. Government Regulators: Overseeing compliance with medical device and pharmaceutical regulations.
  8. Consultants and Advisors: Providing expertise in navigating regulatory challenges in E&L testing and material compatibility.

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