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    Post Market Surveillance SOP & Templates

    We have developed high-quality mandatory Post Market Surveillance SOP, Plan and Report templates 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 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 SOP & Templates 1

    Post Market Surveillance (PMS) Forms / Templates

    Post Market Surveillance Plan: 350 USD

    Template ID: I3C-TEM-32/R2-10/19

    Post Market Surveillance SOP & Templates 1

    Sales Data: 50 USD

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

    Post Market Surveillance SOP & Templates 1

    Data Collection and Analysis: 150 USD

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

    Post Market Surveillance SOP & Templates 1

    Post Market Survelliance Report: 300 USD

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

    Post Market Surveillance SOP & Templates 1

    Customer Feedback Form: 50 USD

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

    Post Market Surveillance SOP & Templates 1

    User Feedback Form: 50 USD

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

    Post Market Surveillance SOP & Templates 1
    Post Market Surveillance SOP & Templates 1

    Attention!!!

    On receipt of payment confirmation, we will send a download link 2-6 hours. The link will be active for six months and in case of any revisions, it will get auto-updated.

    In case of any delay in receiving the link, please write to enquiry@i3cglobal.com with details. We will make sure you will get it.

    Post Market Surveillance (SOP & Templates)