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Starting Starting 17 October 2022
LIVE Online Training Course | 9am - 5:00pm CET
Starting Starting 17 October 2022

LIVE Online Training Course | 9am - 5:00pm CET

Understand the fundamentals of Biocompatibility and gain confidence in adhering to global standards

Course Overview

Biocompatibility is one of the most critical areas when it comes to medical devices: allowing manufacturers to understand how a medical device interacts with the host upon implantation. However, with the global standards being technical and complex, and testing expectations differing per country, it is imperative that those entering the industry gain a comprehensive understanding of these standards.

Guided by Biocompatibility experts Beau Rollins and Marina Daineko, delegates will learn the fundamentals of Biocompatibility and the tools needed to successfully adhere to global standards, including: the history of biocompatibility, ISO-10993, biological evaluations, endpoint tests and global submission requirements.


Gain real-time access to a subject matter expert delivering online training in a structured virtual classroom environment.
Students will learn through:

  • Live interactive sessions
  • Direct interaction with the trainer during live sessions
  • Participation in interactive features within sessions including polls, Q&A, break out rooms, tasks, case studies, and more
  • Interaction with peers during live sessions and through the online forum

Timings and dates are subject to change - final confirmation will be provided with login details. Delegates will receive login instructions two days prior to the course start date. If you have any questions please contact

What will you learn?

Foundations of Biocompatibility

Understand the definitions and history/foundations of Biocompatibility

Requirements of Biological Evaluations

Identify the key components of biological evaluations

Biological Endpoint Reviews

Navigate E&L test requirements

Global Biocompatibility Submissions

Analyse expectations for biocompatibility submissions under FDA, EU MDR and rest of world

Who should attend?

This course has been designed for toxicologists and biocompatibility scientists and experts who are new to the industry or wanting a refresher on the fundamentals of Biocompatibility standards and submissions.