1992 -

Working Towards Harmonization in Medical Device Regulation

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Study Group 3 (SG3) - Quality Systems

Purpose of Study Group

SG3 is responsible for the task of examining existing quality system requirements in countries having developed device regulatory systems and identifying areas suitable for harmonization.

Study Group Details

• Study Group Chair
• Participants
• SG3 Work Plan

Documents

• Proposed Documents - (for review & comments )
• Comments Template - (for use in providing comments on proposed documents)
• Final Documents
• Archived Documents
• Meeting Summaries

Updated 20 November 2007

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