The Post Market Clinical Follow-Up Report (PMCF) is usually compiled after your post market clinical data is collected. The report can be used to hold interim clinical data and serve as an input into the next update of the clinical evaluation report for your medical device. This template covers: – Confirmation of the safety and performance of the device – Identification of, and monitoring previously unknown side-effects and contraindications – Identification and analysis of emergent risks – Ensuring continued acceptability of the benefit-risk ratio – Provision of an overview of the procedure and justifications of PMCF activities covered After purchasing, you will receive a word document that is ready to edit. You will receive a copy of the Post Market Clinical Follow-Up template within 24 hours of payment.

The Post Market Clinical Follow-Up Report (PMCF) is usually compiled after your post market clinical data is collected. The report can be used to hold interim clinical data and serve as an input into the next update of the clinical evaluation report for your medical device. This template covers: – Confirmation of the safety and performance of the device – Identification of, and monitoring previously unknown side-effects and contraindications – Identification and analysis of emergent risks – Ensuring continued acceptability of the benefit-risk ratio – Provision of an overview of the procedure and justifications of PMCF activities covered After purchasing, you will receive a word document that is ready to edit. You will receive a copy of the Post Market Clinical Follow-Up template within 24 hours of payment.