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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.


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PMCF Plan Template

Post Market Surveillance Procedure / SOP

Type : Procedure
Title : Post Market Surveillance Procedure
Document ID : I3C-PMS-01/R2-10/19
Price : $200
Number of Downloads (until 10/2022) : 657

113 reviews

Post Market Surveillance (PMS) Forms / Templates

Type : Templates
Title : Post Market Surveillance Plan
Document ID : I3C-TEM-32/R2-10/19
Price : $350
Number of Downloads (until 10/2022) : 320

69 reviews

Type : Templates
Title : Sales Data
Document ID : I3C-TEM-33/R1-08/19
Price : $50
Number of Downloads (until 10/2022) : 91

25 reviews

Type : Templates
Title : Data Collection and Analysis
Document ID : I3C-TEM-34/R2-10/19
Price : $150
Number of Downloads (until 10/2022) : 23

17 reviews

Type : Templates
Title : Post Market Surveillance Report
Document ID : I3C-TEM-35/R2-10/19
Price : $300
Number of Downloads (until 10/2022) : 431

94 reviews

Type : Templates
Title : Customer Feedback Form
Document ID : I3C-TEM-36/R1-10/19
Price : $50
Number of Downloads (until 10/2022) : 29

09 reviews

Type : Templates
Title : User Feedback Form
Document ID : I3C-TEM-37/R1-10/19
Price : $50
Number of Downloads (until 10/2022) : 31

11 reviews

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We have been in the regulatory consulting business since 1999. After two decades, we have grown to be one of the largest groups, with offices in more than six countries. More than 2000 companies are connected to us in some way and will always be with us in the coming years.

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The files you purchased are not downloaded automatically. After obtaining payment confirmation, you will receive an email within 1-6 hours. (Sundays are days off.)


Our technical experts create the softcopy procedures, templates, and checklists for sale after interpreting and debating guidelines. The briefings or explanations given in each section do not constitute an official or signed contract, and no grievances will be considered. Buyers should keep in mind that the writers are human beings, and there might be a few flaws as interpreted by regulatory authorities or other professional experts in this area.

Refund Policy

We will NOT issue a refund once the softcopy document has been submitted.



Softcopy procedures, forms, and checklists for sale must be updated and filled out according to the scope of the product. We cannot guarantee that simple forms will be accepted by the NB or FDA, but properly filled forms based on our advice will have a better chance of being accepted.


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