This document provides a comprehensive overview of our requirements engineering process. It is designed to help experienced professionals understand how we collect, document, and manage requirements using Azure DevOps. By adhering to this guide, we ensure consistency, traceability, and compliance throughout our projects.
The requirements engineering proicess is tightly bound to the [traceability concept](traceability-concept.md) and the [requirements gathering interview](requirements-gathering-interview.md).
Requirements are work items in Azure DevOps and the summarizing AsciiDoc document is located within the [docs-requirements](https://dev.azure.com/ypsag/ITSandbox/_git/docs-requirements) repository.
Our requirements engineering process is a structured approach that takes us from the initial stakeholder conversations to a finalized set of requirements. We emphasize:
- **Clarity and Testability:** Requirements should be simple statements that are testable. We are writing test cases along with the stakeholder requirements.
- **Traceability:** Maintaining clear links from requirements through to implementation and testing and back.
**Objective:** Manage changes to requirements systematically.
- **Principles:**
- **Immutability of Requirements:** Once a requirement is baselined, it should not be altered. If changes are needed, deprecate the old requirement and create a new version.
Traceability is crucial for tracking requirements through all stages of development. We use a Traceability Matrix to map requirements to other project artifacts. As of now the document is created manually in AsciiDoc format. We aim to automate this process in the future.
- **Requirement ID:** Unique identifier, we are using the Azure DevOps work item id.
- **Requirement Title:** Summary of the requirement.
- **Affected Regulations:** Relevant laws, standards, or regulations. We are using a link to the requirement work item representing the regulation in Azure DevOps.
- **Test Case ID(s):** Linked test cases for validation, we are using the Azure DevOps Test Case id.
- **Communication:** Utilize Azure DevOps **Discussion** section in Work Items for conversations and decisions. Set up notifications for stakeholders to keep them informed of updates.
- **Training:** Familiarize yourself with the Azure DevOps CMMI process template and our customized fields. Stay updated on best practices in requirements engineering.
- **Regulatory Awareness:** Stay informed about regulations relevant to our projects (e.g., GDPR, HIPAA). Consult with compliance officers when in doubt.
- We are a med tech company producing physical devices incl. embedded hardware and software, mobile apps connected via bluetooth and cloud components like user management device management for those mobile apps
- We are the IT department offering IT infrastructure in the Azure cloud for those products. We are not creating the products and we are not responsible for the processes involved to create the products. We are only providing infrastructure for those products and are responsible for IT infrastructure changes.
We have identified the following list of regulations as potentially relevant:
- ISO/IEC 62304 Medical device software - Software life cycle processes
- ISO/IEC 27001 Information technology - Security techniques - Information security management systems - Requirements
- ISO/IEC 27017 Information technology - Security techniques - Code of practice for information security controls based on ISO/IEC 27002 for cloud services
- ISO/IEC 27002 Information security, cybersecurity and privacy protection Information security controls
- ISO/IEC 27018 Information technology - Security techniques - Code of practice for protection of personally identifiable information (PII) in public clouds acting as PII processors
- ISO 14971 Medical devices Application of risk management to medical devices
- ISO 13485 Medical devices Quality management systems - Requirements for regulatory purposes
- FDA 21 CFR Part 820: Title 21 Code of Federal Regulations Part 820 - Quality System Regulation
- FDA 21 CFR Part 11: Title 21 Code of Federal Regulations (CFR) Part 11 - Electronic Records; Electronic Signatures
- ALCOA+ Principles Compliance
You are an expert in the field of requirements engineering in the regulated environment of a med tech company. I need your support in writing requirement.
When writing requirements, use the following format to clearly articulate the need, the stakeholder’s perspective, the desired outcomes, and the rationale. Adhere strictly to this structure:
When [condition or situation triggering the requirement],
As [stakeholder role],
I want [specific actions or outcomes to achieve].
This ensures [reason or benefit for implementing the requirement].
Key Guidelines:
1. Condition or Situation: Clearly state when or under what circumstances the requirement applies. Use "When..." to frame this.
2. Stakeholder Role: Explicitly identify the stakeholder requesting the requirement. Use "As [stakeholder role]..." to reflect the stakeholder's voice.
3. Desired Outcomes: Use "I want..." to specify what the stakeholder expects or desires to be achieved. List actions or outcomes in a concise, actionable manner.
4. Rationale: Use "This ensures..." to explain why the requirement is important or what benefit it provides.