GxP Validation
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Save Time and Effort for Validating Multiple Veeva Vault Releases Every Year
Typically, Veeva Vault undergoes three general releases and several internal releases every year.
Veeva clients get only 4 weeks to adopt a new release. The process includes analyzing impact, scoping and conducting tests, training, and getting approvals of all validations.
With Prana Life Sciences GxP Validation solution our clients can complete this end to end process in less than 4 weeks.
Challenges & Problems
- Adopting rapid Veeva releases is resource intensive and can impact compliance, budget and timelines.
- Conducting end-to-end validation manually is prone to errors, misjudgments and missteps. And most importantly it may not feasible due to tight release schedules.
- Identification of training needs for respective roles.
- Manual risk identification and risk-based testing may lead to incomplete validation testing.
Features (Capabilities)
- 365 value-added validation coverage for both CSA and CSV approaches.
- Automation of identification of risks and training needs.
- Full set of deliverables including templates, forms, training, and SOP.
- AI-powered dynamic test automation for platform features, applications, and new release features
Benefits
- Reduce cost of operations.
- Faster time-to-market.
- Compliant with GxP regulations.
- Extend your competitive advantage.
- Leverage latest and greatest technologies such as gen-AI and ML.
- More testing and more value-addition using critical thinking than just producing piles of paper.
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