SOP Software Problem Resolution#

Classes

IEC 62304:2006 Section

Document Section

B, C

5.6.8

(All)

A, B, C

6.2.1.3

1

A, B, C

6.2.2

(All)

A, B, C

9.1

1

A, B, C

9.2

2

A, B, C

9.3

3

A, B, C

9.5

1

A, B, C

9.6

2

A, B, C

9.7

3

Summary#

This SOP describes how problems concerning our software product(s) are processed, evaluated and fixed.

Process Steps#

1. New Problem Evaluation#

New problems are entered as tickets into <your ticketing system>.

Reported problems can originate from customers, users or company employees. Examples include customer feedback and bug reports.

For each problem report, the following must be entered:

  • Affected medical device and version

  • Severity classification (see below)

  • Problem description incl. instructions to reproduce

We classify the severity of problems in the following categories:

Severity Classification

Description

High

Causes new or changed risks to patients which are unacceptable.

Medium

May cause new or changed risks to patients which are acceptable.

Low

All other problems.

For all problems classified as “Medium” or higher the person responsible for regulatory compliance must be informed who subsequently assesses it based on SOP Incident Reporting.

Under MDD, replace the Person Responsible for Regulatory Compliance with Safety Officer.

Participants

Head of product development

Person responsible for regulatory compliance

Input

Output

New problem

Problem report as <ticket in your ticketing system>

2. Root Cause Analysis and Procedure#

The root cause of the problem is determined (if possible) and a decision is made whether to fix it or not.

We also analyze whether similar problems have occurred in the past and any trends can be discerned. If this is the case, it is noted in the problem report.

Participants

Head of software development

Software developer

Input

Output

Problem report

Problem report updated with cause and procedure

3. Implementation and Verification#

The change is implemented. If the change includes a change to an existing product, it is handled according to SOP Change Management.

After the change has been implemented, the problem report is reviewed whether it has been successfully fixed and can be closed. Closing the problem report is equivalent to successful verification.

Participants

Head of product development

Person responsible for regulatory compliance

Input

Output

Problem report

Resolved/closed problem report

Implemented change