Computer system validation (CSV) is an essential process to ensure all computer systems work as intended as part of the manufacturing process.
Ensuring the integrity, reliability, and availability of hardware and software to support the production of quality products and protect patient safety is critical. Companies accomplish this by verifying the controlled development and implementation of computer systems.
Companies that don’t employ the right strategies, processes, and technology are vulnerable to undesirable consequences such as regulatory issues, defects, time-consuming and costly re-work, and ultimately, patient risks.
Prioritizing adequate planning, preparation, and innovation within your CSV processes can help you avoid these adverse outcomes.
5 Steps to More Efficient Computer System Validation
Are you involved in the validation of computer systems within your company? If so, you know that executing the validation process correctly is equally as important as executing it in a manner that promotes efficiency and scalability.
Read our executive brief to learn about five steps you can take to create a more proactive and pragmatic CSV process.
Let’s Work Together
You can’t solve computer system validation inefficiencies with technology alone. Finding a partner with extensive CSV experience within the constantly changing biopharma and life sciences manufacturing field can make all the difference.
Our life sciences and pharma qualification and validation experts are eager to work with you to develop a proactive CSV plan that prioritizes accountability, saves time, and reduces costs.