July 21, 2022
If you think of validation as a pie, document authoring is 25% of the pie. A DMS can’t address the other 75% of validation activities ValGenesis supports.
June 7, 2022
Explore the top 10 business benefits you'll receive from digitizing your paper-based validation processes with ValGenesis.
May 23, 2022
Speed-to-market is a top priority for CDMOs. Being a digital-first organization gives Theragent a substantial competitive advantage.
May 5, 2022
CSA is achievable under current regulation. If you’re following these 3 core CSV principles, odds are you’re already aligned with the new CSA methodology.
April 21, 2022
When manufacturers rely on paper-based logbooks, they expose themselves to human errors, poor data integrity, and a host of compliance risks.
April 7, 2022
ValGenesis' global user conference brings together customers, partners, experts and employees for an informative, inspiring and interactive experience.
March 22, 2022
ROI study reveals how much time and money customers saved by digitizing their corporate validation processes. Watch the webinar (link in post) to learn more.
January 31, 2022
Is CSA the new CSV? Not exactly. Here's your comprehensive guide to computer software assurance, the FDA's new framework for validating software systems.
January 17, 2018
Manual requirements traceability matrix generation is error-prone and costly due to the resources and time required to maintain them during the validation lifecycle.