Huge shout-out to Maria for delivering such an insightful webinar on the benefits of running CPV in real time!🙌If you missed it, the recording is now available - check it out! 👉hubs.li/Q03vVyg70

INTERPHEX Week Tokyo is just 2 days away, and we’re excited to be attending alongside our partners, Hitachi and VALIDATOR K.K.! Be sure to stop by and meet VAL 🤖 — our AI-powered Validation Assistant that’s redefining the future of validation. 👉hubs.li/Q03w33pY0

Streamlined CPV starts with seamless integration. iCPV™ connects directly to your systems, automating validation and enabling real-time data synchronization - without manual steps or transcription errors. Learn more here👉hubs.li/Q03wgQSh0

Big news, we launched a brand-new website! ✨ Now it’s easier than ever to discover our solutions, find valuable resources, get the latest insights, and connect with our experts - all in one place. Take a look 👉 hubs.li/Q03wpX5l0

Modern AI-driven validation lifecycle solutions are changing the game! With VAL, you can accelerate validation, stay compliant, boost accuracy, and save valuable time. Are you ready to break free from manual bottlenecks? Join our webinar and see how! 👇 hubs.li/Q03wt0ZR0

With ValGenesis’ AI-enabled Validation Lifecycle Suite, costs go down by up to 30% and efficiency goes up, cutting audit prep time by 90%. That’s the power of intelligent automation for CQV. Curious how it works? Check it out! 👇hubs.li/Q03wGvgC0

With ValGenesis Smart GxP™, compliance is no longer a burden but a strategic advantage. 😎 Join Sachin’s webinar to see how industry leaders achieve effortless regulatory readiness, reduce audit stress, and accelerate product launches. 🚀 👉 hubs.li/Q03wH0CJ0

Say goodbye to outdated practices - it's time to embrace digital CQV! 😎 Join our webinar to discover how digital CQV is transforming validation workflows and accelerating the path to Pharma 4.0. Ready to lead the change? Let’s go! 🚀 hubs.li/Q03x2f4P0

An integrated C&Q approach aligns commissioning and qualification efforts - improving compliance, efficiency, and product safety. This two-part series breaks down each phase, so you can see what C&Q is all about. Let’s start with the first two phases. 👇 hubs.li/Q03xdWQX0

Many organizations still rely on fragmented systems to manage their CQV efforts—leading to increased compliance risks and slower project delivery. The solution?💡Unify your validation processes in a single digital platform. Check it out! 👉hubs.li/Q03xv0N70

Say goodbye to outdated CQV practices.👋In our upcoming webinar, we’ll explore how digital CQV is reshaping validation and enabling life sciences organizations to accelerate their journey toward Pharma 4.0. Register now! 👉hubs.li/Q03xDL3Z0

How Inefficiencies in Tech Transfer Drive Up Costs hubs.li/Q03xDS700

Cut audit prep time by 70%, slash validation cycles by 80%, and reduce observations by 90%! 🚀 Yes, it’s possible. Want to know how? Check out our webinar! 👉hubs.li/Q03xPFdW0

Imagine a world where paperwork and repetitive CQV tasks no longer slow you down. With digital CQV, that world is now a reality! Join our webinar to discover how digital transformation is reshaping CQV—and how it empowers you to align with Pharma 4.0. 👉 hubs.li/Q03y1hhN0

INTERPHEX Week Tokyo 2025 was amazing!🎉Huge thanks to our partners Hitachi and VALIDATOR K.K., and to everyone who stopped by - it was unforgettable! Did you meet VAL 🤖, our AI-powered Validation Assistant? 👉hubs.ly/Q03y4Lpj0

We’re redefining the future of digital validation. This journey wouldn’t be possible without the support of our trusted partners. That’s why, together with Morgan Stanley Expansion Capital, we’re excited to announce strategic financing from Bridge Bank. 👇hubs.li/Q03yd4vh0

Last week, we brought you part one of this two-part series, where we explored the first two phases of commissioning and qualification. Now, it’s time for the final chapter - phase 3 and 4. Check it out! 👇 hubs.li/Q03ydyXc0

Say goodbye to spreadsheets and hello to intelligent validation! 🤖Unlock faster, smarter, and compliant operations with AI-powered validation. Join our webinar to discover how intelligent validation is transforming the industry. 👉hubs.li/Q03yrv0j0

Still using paper records or spreadsheets for tech transfers? It’s time to rethink your approach!🚨Our latest blog post explores why - and what you can do instead. 👇 hubs.li/Q03yKT3C0

Did you miss Saurabh’s webinar on Digital CQV and Pharma 4.0? No worries - watch it on demand to see how digital transformation can drive efficiency, ensure compliance, and spark innovation. 👉hubs.li/Q03yTqcX0