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Day 2: IMDRF Guidance Documents In The Works

 
• By Brian Bossetta

Discussions during the second day of the 25th session of the International Medical Device Regulators Forum focused on the establishment of working groups to iron out a plethora of issues for international harmonization.

Working Group
• Source: Shutterstock

Before the 25th session of the International Medical Device Regulators Forum (IMDRF) convened in the nation’s capital on 11 March, Melissa Torres, the FDA’s associate director for international affairs, told Medtech Insight that one of this year’s goals was for the forum’s various working groups to make headway on creating documents to help everyone get on the same page.

“There are documents that will be considered during this meeting, or and new work item proposals that will be considered as well,” Torres said, noting that

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