Good Documentation practices SOP

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P Bankruptcy Provisions for availability of Technical Documentation EU Medical Device Regulations 5
Q Minimal Documentation Method & 4.2 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
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D Swiss Documentation Requirements for Class 1 Medical Device Other Medical Device Related Standards 0
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S Documents belonging to Technical documentation to be stored in one file or spread in the QM system? EU Medical Device Regulations 10
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H Characteristics related to safety - format of documentation ISO 14971 - Medical Device Risk Management 3
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E Technical documentation for IVDD General/ other CE Marking (Conformité Européene) / CB Scheme 3

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