What is DevOps documentation?
What is DevOps documentation?
The scripts which control the automated DevOps processes also serve as a form of documentation. They include information about system, server, and software configuration, and they serve as a detailed generic record of the deployment process.
What is continuous documentation?
Continuous documentation is the process of creating and updating documentation incrementally and as part of the development workflow, ensuring it is in sync with the codebase.
What should be included in technical documentation?
It includes requirements documents, design decisions, architecture descriptions, program source code, and FAQs. User documentation covers manuals that are mainly prepared for end-users of the product and system administrators.
What are the standards of documentation?
Documentation standards
- Documentation process standards These standards define the process that should be followed for document production.
- Document standards These standards govern the structure and presentation of documents.
How do I write a DevOps document?
Best practices for documentation in DevOps
- Eliminate silos. Writers — or other staff tasked with documentation preparation — should be included as a normal and essential element of every development team.
- Collaborate.
- Set documentation requirements.
- Adopt standard tools.
- Automate tools where possible.
What is Doc code?
Docs as code means applying software development processes and tools to technical documentation. We write our content in a plain text format using a text editor rather than a markup language like XML and a content management system.
What is the structure of a technical documentation in Canada?
In Canada, the structure of a technical documentation is based on the STED structure. The Canadian authority has also published an own model for this purpose. Always applicable: manufacturers must be precisely informed about the regulatory requirements related to the TD in the country, where they want to obtain approval for a medical device.
What is STED (summary technical documentation)?
A certain point of reference in terms of structure is the so-called STED (Summary Technical Documentation), which was created by the Global Harmonization Task Force (GHTF), the predecessor of today’s International Medical Device Regulators Forum (IMDRF). Its aim was to develop global unique applications for approval for medical devices.
What are the requirements for technical documentation under the MDR?
However, many requirements for the technical documentation by the MDR are already partly known from standards, such as DIN EN ISO 13485, DIN EN ISO 14971 or DIN EN 62366-1. Often these are already applied in the companies concerned. Thus, it is within the bounds of feasibility, under the MDR, to apply these requirements to TD.
How has the comprehensiveness and requirements of the technical documentation increased?
Although this short exposition above is already a summarised version, it clearly illustrates how the comprehensiveness and requirements of the technical documentation have increased. An important fact is, that with the new MDR the EU Commission is able to change the requirements for the TD in accordance with technical progress, if necessary.
