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HCL Technologies

Medical Devices-Clinical Evaluation Reports

Medical Devices-Clinical Evaluation Reports

This whitepaper describes MEDDEV 2.7.1 Rev. 4 new requirements and approaches and align to the new European MDR compliances. HCL understand the new requlatory requirements and developed its own process flow and checklists .These process flow and checklist are guide to undertand and helps the Clinical analyst and evaluator to prepare a good quality clinical evaluation reports.

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We will treat any information you submit with us as confidential.