Extractables & Leachables 2025 Webinar

Place: Online

Date: May 28-29, 2025
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 Extractables & Leachables 2025 Conference!

The Extractables & Leachables 2025 Webinar is a premier two-day event bringing together experts, industry leaders, and key stakeholders to explore critical advancements in extractables and leachables (E&L) testing and regulatory compliance. Designed to address the latest developments in E&L testing, the conference covers essential topics such as regulatory frameworks, advanced analytical techniques, material compatibility, and toxicological considerations. Attendees will engage in practical discussions on best practices for minimizing E&L risks and explore the impact of emerging technologies on E&L testing and the future of material safety. This event serves as a platform to share knowledge, gain insights, and stay ahead of evolving industry needs, ensuring the safety, stability, and compliance of medical devices and drug delivery systems.

The conference contains

10+ expert-led sessions

Q&A Sessions

Panel discussion

Post-webinar materials

Certificate of Attendance

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!

Our Previous Speakers:

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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Extractables & Leachables in Medical Devices 2025 Webinar

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