2nd June, 2021 | 2pm to 2:30pm EST
Ready to learn how Life science companies can accelerate their application development cycles and still address all system validation requirements.
The life sciences industry is undergoing major change in terms of adopting agile methodology which has enabled the development cycle time to be reduced from months to weeks. However, Life Sciences organizations still have to meet regulatory compliance requirements like FDA 21 CFR Part 11.
With all these challenges it is imperative that test management and testing execution are automated to improve validation processes, accelerate software release cycles, and lower costs while also meeting validation requirements for clear traceability and audit trials.
Apexon’s solution ensures improved efficiency and accuracy of CSV (computer systems validation) for an FDA regulated environment. This is achieved by way of web-based approval processes which integrate electronic signature for the approval workflows, maintain audit history & traceability and test automation.
First Speaker’s Brief Profile
Second Speaker’s Brief Profile