RAPS WEBINAR
Automated Validation Platforms Ensure Compliance with Greater Efficiency and Consistency
In this panel discussion presented by RAPS, a panel consisting of R&D, Clinical Research, Regulatory Affairs and IT professionals discuss their recent experience implementing a SaaS Computer System Validation (CSV) platform. As life sciences companies take on more software to support growth, it leads to a constraint on internal resources. Utilizing an automated validation platform ensures compliance with greater efficiency and consistency.
Featured Resources
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WHITEPAPERHow to Transition to Validation 4.0The International Society for Pharmaceutical Engineering (ISPE) is providing guidance and best practices to achieve its vision for Pharma 4.0, a future state where organizations leverage the full potential of digitalization to provide faster innovations for the benefit
of patients.Read More
of patients.Read More
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ARTICLEThree Ways Life Sciences CIOs Can Prioritize Validation 4.0For life sciences chief information officers (CIOs), digital validation is often treated as an afterthought. However, validation in life sciences is an integral part of the foundation of any life sciences business.Read More
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PRESS RELEASESware Partners with BenchlingWe are excited to announce that Sware is partnering with Benchling to accelerate digital R&D transformation for biotechs globally — by enabling adoption of modern life sciences validation software, purpose-built for science.Read More
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Res_Q was built to serve the unique, complex requirements around CSV for GxP systems. Leverage our intelligent validation automation platform and our deep compliance expertise to your benefit — reach out today to schedule a no-pressure session. We’re here to help you.