Since the paradigm shift in 2000, international standards such as ISO 9001 have taken an increasingly process-oriented approach to the design of quality management. Our documentation tool „d.velop life sciences | process documentation“ takes account of this fact and helps to document, structure and visualize the processes in your company simply and uniformly. Connect your respective business processes with each other and link the processes with already existing documents from the d.3ecm DMS and d.velop life sciences QMS. At the same time, a process manual can be automatically generated within the process documentation software in several formats based on the stored process data.
How do you benefit from the Process Documentation software?
Some features of the Process Documentation
Regulatory requirements that are met
Would you like a live webcast of the software?
Get a live insight into the possibilities of process-oriented documentation in just 30 minutes with a sample use case in the process documentation software. Learn how you can document, structure and visualize your processes in your company easily and uniformly with the solutions by d.velop Life Sciences.
33 Good reasons for a cooperation with d.velop LS
You’re not convinced yet? Find out about 33 good reasons speaking for a cooperation with d.velop Life Sciences GmbH. We will show you reasons from the provider’s point of view, from the software point of view and other general reasons that distinguish us.
Frequently asked questions (FAQs) about Process Documentation
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The Process Documentation is a component of the d.velop life sciences solution suite. Each product is powerful on its own, but when used together they are even better.
Whether work / process instructions (SOPs), process descriptions, test specifications or other types of documents — you can create, revise and sign them all digitally with this module.
Extend the “Document Control” module to actively plan and record the qualifications of your employees with our training management.
QM Workflows (Complaint | DC | CAPA | CC)
Digitalize your ISO processes. Control your production-related QM processes using digital workflows.
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