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Medical Device System Software Validation Documents

Siemens Dreamer Siemens Dreamer
Siemens Dreamer
As I discussed in my last blog, software used as a platform to support the manufacture of product or in the product quality management system (QMS) must be validated (as required by 21 CFR §820.70(i)). The process is the same process used to develop design controls for a medical device without the requirement for compliance with ISO 62304 [white paper: Achieve Fast Compliance with IEC 62304]. Larger medical device firms usually assign this task to their IT department.
Documents typically used in establishing the Software Validation are as follows: The Software Validation Plan A document outlining the project milestones, deliverables and participant responsibilities. System Work Instructions Work instructions to be used in the software validation effort The Software Requirements Specification (SRS) This document describes the details of the user needs, system, and design requirements, physical hardware requirements, design architecture (including a network diagram), training, and integrations with other systems. Part 11 compliance, safety, and risk analysis should also be part of building the inputs for V&V. The image below describes the design element traceability required for this task.
Software Verification Protocol Test protocol for verification of software requirements. Includes all verification test cases. Software Validation Protocol Test protocol for Validation of software user needs.  Includes all validation test cases. Software V&V Trace Matrix Includes the traceability from Inputs (User needs and software requirements) to test cases.  This progression should follow the FDA design guidance flow chart shown below.
  Risk Analysis Typically a user risk FMEA used to analyze potential of software failure to cause user harms. Software V&V Report Executed test scripts, and tester training records. Regulators have a very specific understanding of the documentation related to software validation. Consider how these documents, which are really containers for your design inputs, traceability and evidence will be compiled and presented to product stakeholders. Polarion is a great tool for creating requirements in the context of documents familiar to regulators. Let us show you how to author requirements in the context of your documents.