# Post-Market Clinical Follow-Up Plan (PMCFP)

Author: Sven Piechottka
Published: 2023-08-02
Updated: 2024-04-26
Source: https://openregulatory.com/document_templates/post-market-clinical-follow-up-plan-pmcfp

---

Post-Market Clinical Follow-Up Plan (PMCFP)
This document is used to plan all post-market clinical follow-up activities for the <name of the medical
device].
Product information
Parameter	Description	
Product or trade name:		
Model and type:		
Intended purpose:		
Context
Check out this guidance document which may further help you to fill out the template: MDCG 2020-7
Post-market clinical follow-up (PMCF) Plan Template: A guide for manufacturers and notified bodies
The post-market clinical follow-up plan is compiled along with concluding the clinical evaluation and is based
on the clinical evaluation report. Following Annex XIV MDR, it specifies the methods used to collect and
evaluate clinical data with the aim of:
confirming the safety and performance of the device throughout its product life cycle,
identifying previously unknown side-effects and monitoring the identified side-effects and contraindications,
identifying and analyzing emergent risks on the basis of factual evidence,
ensuring the continued acceptability of the benefit-risk ratio referred to in sections 1 and 9 of annex I
MDR, and
identifying possible systematic misuse or off-label use of the device, with a view to verifying that the
intended purpose is correct.
1. Activities related to PMCF: general and specific methods and procedures
This section outlines post-market activities for PMCF, detailing general and specific methods/procedures
related to the product's scope. It also covers the purpose of each activity, the rationale behind chosen
methods, and anticipated limitations. Activity timelines are to be defined quarterly or yearly.
Examples of PMCF activities include:
Manufacturer Device Registry: Specific to the device type or medical device group, include a brief
plan description, specifying quality and quantity data based on device risk.
PMCF Studies: Details study plans, encompassing design, sample size, endpoints, and
inclusion/exclusion criteria.
Surveys: Describes planned surveys for collecting information on the use of the medical device.
The overarching aim is to streamline post-market activities, ensuring comprehensive data collection,
analysis, and validation.
1.1 General methods and procedures
According to the MDR, Annex XIV, 6.2 The PMCF plan shall include at least:
(a) the general methods and procedures of the PMCF to be applied, such as gathering of clinical experience
gained, feedback from users, screening of scientific literature and of other sources of clinical data;
Below are two examples provided:
Method 1	<Literature Review>	
Description:	<Literature search as defined in the search protocol of the CER>	
Search period:	<Beginning from last update of CER until Month/Year>	
Objective:	<Confirming the findings of the initial Clinical Evaluation Report and identifying new potential benefits and risks>	
Search Strategy:	<Copy paste your search strategy from the CER here>	
Rationale and known limitations of the activity:	<Address device risk, the novelty of the product and/or of the clinical procedure, the sufficiency of clinical data in the CER & the objective of this method>	
Method 2	<Feedback from users or patients>	
Description:	<Describe the survey>	
Search period:	<State the survey periode here>	
Objective:	<Describe the objective of your survey>	
Additional information	<Countries, sponsor, survey sides...>	
Rationale and known limitations of the activity:	<Address device risk, the novelty of the product and/or of the clinical procedure, the sufficiency of clinical data in the CER & the objective of this method>	
1.2 Specific methods and procedures
According to the MDR, Annex XIV, 6.2 The PMCF plan shall include at least:
(b) the specific methods and procedures of PMCF to be applied, such as evaluation of suitable registers or PMCF studies;
Method 3	<PMCF Study>	
Description:	<Describe the study>	
Search period:	<State the study periode here>	
Objective:	<Describe the objective of your study>	
Additional information	<Countries, sponsor, survey sides...>	
Rationale and known limitations of the activity:	<Address device risk, the novelty of the product and/or of the clinical procedure, the sufficiency of clinical data in the CER & the objective of this method>	
Method 4	<Device registry>	
Description:	<Database search as defined in the CER>	
Search period:	<Beginning from last update of CER until Month/Year>	
Objective:	<Confirming the findings of the initial Clinical Evaluation Report and identifying new potential benefits and risks>	
Search Strategy:	<Copy paste your search strategy from the CER here>	
Rationale and known limitations of the activity:	<Address device risk, the novelty of the product and/or of the clinical procedure, the sufficiency of clinical data in the CER & the objective of this method>	
2. Reference to the relevant parts of the technical documentation
In this segment, the manufacturer must incorporate citations to pertinent details from both the clinical
evaluation report and the risk management file. These references are subject to analysis, follow-up, and
assessment within this plan. Alternatively, the manufacturer must explicitly declare if there is no relevant
information from the clinical evaluation report and/or the risk management file that requires consideration
in this plan.
2.1 Clinical Evaluation Report (date and version)
Relevant information to be further analysed and monitored:
<Describe what needs to be analysed>
Example: The clinical data gathered and evaluated as a result of this PMCF plan will be used to update and
verify the chapters 11.6 (literature summary and conclusion), 12 (clinical experience data), 13
(risk-benefit assessment) and the conclusion of the CER. The literature will furthermore be searched for
similar devices with a focus on associated risks and the state of the art.
No relevant information from the clinical evaluation report to be considered in this plan
2.2 Risk Management File (date and version)
Relevant information to be further analysed and monitored:
<Describe what needs to be analysed>
Example: Clinical data will be used to ensure the ongoing appropriateness of identified hazards, hazardous
situations, harms, their frequency and severity estimations in the risk assessment & risk
control. Furthermore, the data including information on similar devices shall be evaluated to identify
potential emerging risks in the risk assessment & risk control.
No relevant information from the risk management file to be considered in this plan
3. Evaluation of clinical data relating to equivalent or similar devices
In this section, the manufacturer is required to compile information on equivalent or similar devices, the
clinical data of which will be subsequently assessed and presented in the PMCF report. It is important to
highlight that PMCF data, aimed at demonstrating ongoing safety and performance, should primarily originate
from the specific device under evaluation. While data from equivalent or similar devices may be utilized—for
instance, to update information on the state of the art or to identify and further evaluate relevant safety
outcomes—the selected devices must remain consistent throughout the technical documentation. It is essential
to specify whether the chosen device is confirmed to be equivalent or is categorized as a similar
device. Each listed device should include a clear reference to the relevant sections of the Clinical
Evaluation Report (CER).
The following equivalent or similar devices have been chosen and the clinical data will subsequently assessed:
Parameter	Equivalent / similar device 1	Equivalent / similar device 2	
Product name of equivalent / similar device			
Intended purpose			
Intended users			
Intended patient population			
Medical condition			
Indication			
Reference to clinical data evaluation in the CER (date, version and location in the text)			
4. PMCF evaluation report
The findings of the PMCF will be summarized in the PMCF Evaluation Report that is part of the clinical
evaluation report and the technical documentation.
Template Copyright openregulatory.com (https://openregulatory.com). See template
license (https://openregulatory.com/template-license).
Please don't remove this notice even if you've modified contents of this template.