Post Market Surveillance SOP & Report Template
Our experts developed Post Market Surveillance Report Template, SOP, and Plan in-line with EN ISO 13485:2016, Section 8.2.1 and Meddev NB-MED/2.12/Rec.1 guideline. During the preparation of the Medical Device CE Marking MDR Technical File, the clinical evaluation report should be concluded with the help of Post Market Surveillance (PMS) Procedure/SOP, Plan and Report with its conclusion.

Post Market Surveillance Procedure / SOP
Type : Procedure
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Post Market Surveillance (PMS) Forms / Templates
Type : Templates
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Type : Templates
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Type : Templates
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Type : Templates
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Type : Templates
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Type : Templates
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