Active market monitoring - We take over these tasks and develop appropriate Post-Market Surveillance strategies for your medical device. As a result, we can identify possible complications and trends early and improve the overall safety of medical devices, which are already on the market.


We focus on your needs.

Do you need a PMS plan for the CE marking of your product?

Do you regularly need PSURs or PMS reports in accordance with current regulations?

Has the Notified Body revealed any deficiencies concerning your documentation?

Are you looking for support in post-market surveillance?

Do you need additional human resources?

Are you looking for external know-how and independent expertise?


We have extensive experience in selecting appropriate post-market safety and performance monitoring activities and finding the appropriate measures for your medical device.

Post-Market Surveillance at a glance

Depending on your requirements our market monitoring activities comprise various modules.


Projekt Kick-off

First, we work with you to define the scope and strategic approach and agree on a timeframe, including any reporting obligations that must be met. The exchange of all necessary information takes place. In this phase, we will exchange all necessary information.


Post-Market Surveillance Strategy

A strategy is developed to meet the requirements of Regulation (EU) 2017/745 and, if requested, ISO/TR 20416.


Post-market surveillance plan (PMS plan)

Together with you, we define in the PMS Plan the best methods to ensure the collection of appropriate data from reactive and proactive activities and plan all steps up to the report.


Identification of PMS data

According to the defined methods and data sources we carry out the necessary research for your medical device. This step includes gathering data as well as documenting all search activities.


Analysis of the data

Based on the agreed criteria, we analyze both quantitatively and qualitatively the collected data of your products and also of similar medical devices – e.g. from regulatory safety databases, literature searches or even surveys and complaints.


Initiation of measures

Should the analyzed data show that corrective or preventive measures are necessary, or even measures in the field, we will work with you to implement these within the framework of the legal requirements. This includes compliance with any reporting deadlines.


Periodic Safety Update Report (PSUR)

We regularly prepare the PSUR for your Class IIa, IIb or Class III products. We are also happy to prepare the post-market surveillance report (PMSR) for your Class I devices. We ensure that the reports are available for your documentation (e.g.: the CER or the SSCP) on time.

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Regular PMSR/PSUR updates

We support you in the regular data collection, analysis and preparation of PSURs or PMS reports for your medical devices.


GAP Analysis

We thoroughly review your PMS documentation. Depending on your individual needs, we either work with your templates or use our tried and trusted ones.