Post Market Surveillance Procedure and Template

We have developed high quality Mandatory Post Market Surveillance Procedure and Paln template in line with EN ISO 13485:2016, Section 8.2.1 and meddev NB-MED/2.12/Rec1 guidelines.

During the preparation of Medical Device CE Marking Technical File, the clinical evaluation report should be concluded with the help of Post Market Surveillance (PMS) Procedure / SOP, Plan and Report with conclusion.

Post Market Surveillance (PMS) 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

Sales Data: 50 USD

Template ID: I3C-TEM-33/R1-08/19

Data Collection and Analysis: 150 USD

Template ID: I3C-TEM-34/R2-10/19

Post Market Survelliance Report: 300 USD

Template ID: I3C-TEM-35/R2-10/19

Customer Feedback Form: 50 USD

Template ID: I3C-TEM-36/R1-10/19

User Feedback Form: 50 USD

Template ID: I3C-TEM-37/R1-10/19



Attention!!!

On receipt of payment we will send DROPBOX link with purcheased file in 1-2 hours. The DROPBOX link will be active for six months and if any revisions will autoupdated. You have the flexibility to edit and modify the file as you like.

In case any delay in receiving the word files, please write to enquiry@i3cglobal.com with fund transaction ID. Our team will take care for sure.

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