We discuss recent changes to the ISO 10993-18 and the upcoming changes to 10993-17 and how they impact medical device makers in particular with toxicology assessments.

A focus is given to how these changes encourage a more unified approach to the process as a whole and we will present on the benefits of assessing both the -17 and -18 components of this standard in collaboration.

What you can learn from this webinar:

• How -17 and -18 work together and how they fit with other parts of ISO 10993
• How the TRA benefits companies
• Good practices for success
• The enhanced importance of collaboration.

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