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
Post Market Surveillance Procedure: 200 USD Procedure ID : I3C-PMS-01/R2-10/19 |
Post Market Surveillance (PMS) Forms / Templates
Post Market Surveillance Plan: 350 USD Template ID: I3C-TEM-32/R2-10/19 |
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Sales Data: 50 USD Template ID: I3C-TEM-33/R1-08/19 |
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Data Collection and Analysis: 150 USD Template ID: I3C-TEM-34/R2-10/19 |
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Post Market Survelliance Report: 300 USD Template ID: I3C-TEM-35/R2-10/19 |
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Customer Feedback Form: 50 USD Template ID: I3C-TEM-36/R1-10/19 |
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User Feedback Form: 50 USD Template ID: I3C-TEM-37/R1-10/19 |
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