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REPORT OF THE SG1 MEETING HELD FROM 10th TO 12th MAY, 2009IN TORONTO, ONTARIO, CANADAAttendeesChair Ginette MichaudViceChair Benny North America Mark Wilkerson FDA, USA Maria Carrillo Health Canada
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Who needs ghtf study group 1?

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GHTF Study Group 1 is needed by individuals who wish to contribute to the exchange of information and expertise in the field of medical devices.
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GHTF Study Group 1 is a group within the Global Harmonization Task Force that focuses on the regulation of medical devices.
Medical device manufacturers and distributors are required to file GHTF Study Group 1.
To fill out GHTF Study Group 1, companies must provide detailed information about their medical devices and compliance with regulations.
The purpose of GHTF Study Group 1 is to ensure the safety and effectiveness of medical devices through harmonized regulations.
Information such as device classification, technical specifications, labeling, and clinical data must be reported on GHTF Study Group 1.
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