Published on April 20, 2023
Reading time: -- minutes
Last updated on November 4, 2024
When we talk about software, the saying “garbage in garbage out” applies both for data and its requirements. And if you write a poor user requirements specification, the result will be a poor software.
It’s not a wild conclusion: feeding a software with bad data will result in badly processed data.
So, with this post, we want to give you some tips about what we think is the proper way to write your URS and its application in CSA. Let’s start!
First, we need to look into the GAMP® 5 reference for the SDLC (Software Development Life Cycle) which is the ASTM E2500.
In there, it clearly states that the foundation of the requirements specification document is based upon product knowledge, process mapping and understanding, regulatory requirements and company quality requirements.
It’s actually a key point: it provides the software developer with a clear statement of what the computer system should do.
Let’s think outside the CSA box for a second. Pretend you are ordering a yakisoba, but you don’t like onions. Would you forget to tell the cook that you don’t eat onions? How would the cook know your preference?
Here we have the same situation.
The software developer can’t guess what you need. In fact, he doesn’t have the obligation to understand your products, processes, regulatory requirements, and quality requirements. Your job is to make them clear to them.
We prepared a few tips to help you improving your user requirements specification:
Of course, this is not a complete list of best practices. But we think that it is a good starting point.
It’s important to involve all the key areas in your company so that you can provide the most accurate answers to the following:
If you want to know more about how can we help you managing and improving your computer system validation, check our CSV/CSA solution and don't hesitate to reach out.
In this blog post, we will give you all the steps about how to create a PACM protocol and how ICH Q12 supports you in it.
By Ricardo Leandro
Read
In this blog post, we'll give you some tips that help you setting up a Digital CPV plan in only three steps.
By Sofia Santos
Read
If you’re following these 3 core principles, odds are you’re already aligned with the FDA's computer software assurance (CSA) methodology.
By Lisa Weeks
Read