Medical Device Quality Assurance and Compliance Professionals

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6. Laboratory Notebook Control

6. Laboratory Notebook Control

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7. PROCEDURE: Device Master Record (DMR)/ Medical Device File (MDF)

7. PROCEDURE: Device Master Record (DMR)/ Medical Device File (MDF)

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7. FORM: Device Master Record (DMR)/ Medical Device File (MDF)

7. FORM: Device Master Record (DMR)/ Medical Device File (MDF)

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9. PROCEDURE: Design Control Template

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9. FORM: Design Control Project Initiation

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9. FORM: Design Control Phase Review & Approval

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9. FORM: Design Control Project Design & Development Plan

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9. FORM: Design Control Customer Requirements

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9. FORM: Design Control Product Specification

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9. MATRIX: Design Control Requirements & Traceability

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15. Engineering Evaluation, Design Verification & Validation

15. Engineering Evaluation, Design Verification & Validation

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20. PROCEDURE: Supplier Management Program

20. PROCEDURE: Supplier Management Program

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20. FORM: Supplier Quality System Questionnaire

20. FORM: Supplier Quality System Questionnaire

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20. FORM: Calibration Service Provider Questionnaire

20. FORM: Calibration Service Provider Questionnaire

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20. FORM: Test Laboratory Service Provider Questionnaire

20. FORM: Test Laboratory Service Provider Questionnaire

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20. FORM: Supplier Status (Add/ Change/ Remove) & Approval

20. FORM: Supplier Status (Add/ Change/ Remove) & Approval

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37. Statistical Techniques

37. Statistical Techniques

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