OpenRegulatory Template

SOP Vigilance

ISO 13485:2016 Section Document Section
8.2.3 All
Medical Device Regulation Document Section
Art. 87 All

Regulatory references: check MEDDEV 2.12./1 for guidance on this topic. As a German manufacturer, you are also subject to national law which lays out more specific requirements (note that in preparation for MDR, the Medizinproduktegesetz (MPG) was replaced by the Medizinprodukte-Durchführungsgesetz (MPDG) and the Medizinprodukte-EU-Anpassungsverordnung (MPEUAnpV) replaced the old Medizinprodukte-Sicherheitsplanverordnung (MPSV)).

Summary

This SOP describes how we handle (potentially) serious incidents and field safety corrective action (FSCA). It outlines how we follow the requirements for reporting to competent authorities and necessary immediate action.

General Considerations

Reportable Serious Incident

An incident is defined as any malfunction or deterioration in the characteristics or performance of a device made available on the market, including use-error due to ergonomic features, as well as any inadequacy in the information supplied and any undesirable side-effect.

Any incident that our organization becomes aware of is reportable, if one of our medical devices could be its cause and if it fulfills the definition of a serious incident as outlined in this process. Potentially serious incidents are assessed based on our respective template form for incident assessment [reference document ID here].

A serious incident is defined as “any malfunction or deterioration in the characteristics and/or performance of a device, as well as any inadequacy in the labeling or the instructions for use which, directly or indirectly, might lead to or might have led to the death of a patient, user or other person or to a serious deterioration in their state of health or a serious public health threat” (see MDR Art. 2 and MEDDEV 2.12./1). Examples are therefore (non-exclusively): * malfunctioning (e.g. a software bug) of one of our medical devices * incorrect labeling, instruction for use or advertising material * usability deficiency causing a misuse

A serious deterioration in state of health results in at least one of the following: * life-threatening illness or injury * permanent impairment of a body structure or a body function * hospitalization or prolongation of patient hospitalization or a condition which requires medical or surgical intervention to prevent any of the above * chronic disease * any indirect harm as a consequence of an incorrect diagnostic result when used within manufacturer’s instructions for use

Note that: not all incidents lead to death or serious deterioration in health. The non-occurrence of such a result might have been due to fortunate circumstances or to the intervention of healthcare personnel. It is sufficient that: (a) an incident associated with a device happened, and (b) the incident was such that, if it occurred again, it might lead to death or serious deterioration in health.

Field Safety Corrective Action (FSCA)

A field safety corrective action (FSCA) is an action taken to reduce a risk of death or serious deterioration in the state of health associated with a device that is already placed on the market. Such actions, whether related to direct or indirect harm, should be reported and informed about via a field safety notice. FSCAs can include (non-exclusively):

Reporting Timescale

All report times refer to when the national responsible authority must first be notified. In case of uncertainty whether the incident has to be reported or not, it is reported within the above deadlines.

Responsible Authorities

Incidents are reported to the authority of the country in which the reportable incident occurred:

Germany:

Spain:

Netherlands:

Poland:

Other national authorities:

More contact data can be found on the website of the European Commission: https://ec.europa.eu/health/medical-devices-sector/new-regulations/contacts_en

FSCA is reported to the authorities in the countries in which the FSCA is carried out, including incidents which occurred outside of the European Economic Area (EEA) but resulted in a recall within European countries.

In parallel to reporting incidents to responsible authorities, our Notified Body is informed where applicable in respect to the applied conformity assessment procedure.

Process Steps

1. Documentation and Immediate Action

Any employee of the company that obtains knowledge of an event with a potentially negative impact on the state of health shall immediately notify the Person Responsible for Regulatory Compliance (PRRC) to initiate this process.

However, input to this process may arrive through multiple input channels (see below). Input channels must be checked regularly, for example, throw continuous post-market surveillance cycles (see process for post-market surveillance).

In a first step, the PRRC opens a CAPA to document the respective event. Where necessary, immediate action is initiated without undue delay as part of the CAPA process.

Participants
Person Responsible for Regulatory Compliance (PRRC)
Input Output
Event with a potentially negative impact on the state of health Documented incident and initiated immediate action where necessary

2. Investigation of Causal Relationship

Secondly, the PRRC investigates the root causes of the event to determine if there is a causal relationship between the use of the medical device and the event. The investigation is documented as part of the CAPA process.

If there is no causal relationship, the event is not considered a reportable serious incident. In such cases, the PRRC proceeds with para. 5 to assess if FSCA is required nevertheless (for example, to prevent the occurrence of reportable events).

Participants
Person Responsible for Regulatory Compliance (PRRC)
Input Output
Documented incident Documented evaluation of causal relationship

3. Evaluation as Reportable Incident

If there is a relationship, the PRRC evaluates if the event qualifies as a reportable serious incident by filling out the incident assessment form. Only serious incidents and FSCA must be reported (Art. 87 MDR). In the case of uncertainty, the event is always reported as a serious incident.

Where it is determined that the incident is not a serious incident or is an expected undesirable side-effect, which will be covered by trend reporting in accordance with the process for post-market surveillance, an explanatory statement must be documented in the incident assessment form.

Participants
Person Responsible for Regulatory Compliance (PRRC)
Input Output
Documented incident and causal relationship Documented evaluation as a reportable incident

4. Reporting of Incidents and Field Safety Corrective Action (FSCA)

Within the applicable reporting timescale (see general considerations above), the PRRC informs the competent national authority about the event using respective reporting forms. The PRRC compiles and provides a report with all information required and available at the time.

If applicable, a copy of the report is sent to the Notified Body involved in the conformity assessment procedure of the device.

Participants
Person Responsible for Regulatory Compliance (PRRC)
Input Output
Completed evaluation of the incident Completed reporting to authorities (and Notified Body)

5. Initiate Field Safety Corrective Action (FSCA)

Based on a risk and root cause analysis of the event, the PRRC decides if field safety corrective actions (FSCA) are required to reduce existing risks (note: FSCA may also be required to prevent the occurrence of reportable events). Possible FSCAs are described as part of the general considerations of this process.

Before actions are taken, we identify affected users / customers and inform them about such actions as part of a field safety notice (FSN). The FSN is written in the language of the respective country and must at minimum include:

A copy of the FSN shall be archived. Customers confirm the receipt of FSNs as well as the implementation of recommended actions. If a customer does not respond, at least three attempts for delivery should be made. It is also documented as part of the CAPA if all attempts to inform a customer were unsuccessful.

For B2B customers of our devices, respective contact details for vigilance purposes must be documented as part of CERT-LIS-DEV. For B2C customers, contact details which allow unique identification of end users must be stored separately for every device.

All FSCA are documented as part of the CAPA and must be reported to competent national authorities as described in the previous para. 4.

You may want to consider a separate process regarding the handling of non-conforming products. This process would entail labeling instructions for respective product code and instructions for employees handling those products.

Participants
Person Responsible for Regulatory Compliance (PRRC)
Input Output
Risks resulting from incident Implemented FSCA, Reporting of FSCA to authorities

5. Verification and Evaluation of Effectiveness

The effectiveness of implemented FSCAs is evaluated as part of the CAPA. As soon as the CAPA is closed, a final report is sent to the responsible authorities to verify that all actions taken are deemed sufficient for completion.

All incident records shall be archived as part of the QMS.

Participants
Person Responsible for Regulatory Compliance (PRRC)
Input Output
Implementation of FSCA Final incident report and closed CAPA

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