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Medical Devices (21 CFR Part 820)

Medical Devices (21 CFR Part 820)

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  1. dosumi

    820.40 document controls

    dosumi, Aug 7, 2015
    Replies:
    5
    Views:
    2,025
    Gert Sørensen
    Sep 8, 2015
  2. Tiffany Detzel

    Supplier Audit Question

    Tiffany Detzel, Nov 8, 2022
    Replies:
    6
    Views:
    2,962
    andic
    Nov 9, 2022
  3. QAengineer13

    Regulatory Document Structure For NPI

    QAengineer13, Feb 23, 2016
    Replies:
    6
    Views:
    1,925
    QAengineer13
    Feb 25, 2016
  4. Lee G.

    Quality Plan (FDA) requirement

    Lee G., Aug 21, 2015
    Replies:
    7
    Views:
    2,588
    Marcelo Antunes
    Aug 27, 2015
  5. Abdullah

    Assembly and Packaging areas separation ??!!!

    Abdullah, Dec 22, 2015
    Replies:
    9
    Views:
    1,880
    Pads38
    Jan 4, 2016
  6. MKenn

    Are Capability Studies a regulatory requirement ?

    MKenn, Mar 3, 2017
    Replies:
    10
    Views:
    2,345
    Vintage Goose
    Mar 9, 2017
  7. QAengineer13

    Design Reviews

    QAengineer13, Dec 18, 2015
    Replies:
    10
    Views:
    2,018
    MCW8888
    Dec 24, 2015
  8. MarkMeer

    Justifying NOT following an FDA guidance?

    MarkMeer, Jan 5, 2016
    Replies:
    12
    Views:
    2,667
    MarkMeer
    Jan 9, 2016
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