USDM Life Sciences

Overcomplicated workflows are quietly undermining compliance in life sciences. Extra approvals. Disconnected systems. Manual handoffs. What starts as “playing it safe” can create costly delays and audit risk. In our latest blog, see how ProcessX helps Quality teams: 🔹 Eliminate redundant steps through risk-based workflow design 🔹 Integrate QMS, LIMS, and document systems 🔹 Cut deviation cycle times by over 70% 🔹 Stay audit-ready with CSA-aligned, GxP-configured workflows 🔗 Read the blog: https://bit.ly/42PpjLV #LifeSciences #ProcessX #DigitalQuality #Compliance #AuditReadiness #WorkflowAutomation #QualityExcellence

Pharma 4.0 is here — but disconnected workflows are holding life sciences organizations back. As manufacturers accelerate toward digital, intelligent, and adaptive operations, outdated manual processes between MES, LIMS, and QMS continue to slow progress and increase compliance risk. ProcessX by USDM closes the gap. 🔹 Rapidly digitalizes deviation, CAPA, change control, and training workflows 🔹 Seamlessly integrates with existing systems 🔹 Delivers CSA-enabled, GxP-ready automation 🔹 Drives measurable outcomes — including 30% faster batch release and 22% fewer deviations Let’s build a future where digital quality enables innovation — not delays it. 🔗 Read the blog: https://bit.ly/42PnqPm #Pharma40 #ProcessX #LifeSciences #DigitalTransformation #USDM

🌐 Hybrid cloud isn’t just a tech upgrade — it’s a strategic shift. In regulated life sciences, staying compliant while scaling innovation is no small feat. Hybrid cloud architectures and integration services are helping organizations do both. In our latest blog, we explore how forward-thinking teams are using hybrid models to: ✅ Secure sensitive data while scaling operations ✅ Streamline research, clinical trials, and manufacturing workflows ✅ Ensure continuous compliance across global regulations 🔗 Read the blog: https://bit.ly/4jV1fO4 #LifeSciences #HybridCloud #DigitalTransformation

📢 By early 2026, all applicable medical devices must be fully registered in EUDAMED—but many manufacturers will need to comply even sooner. Now is the time to build a strategy that’s not just compliant, but future-ready. Join experts from USDM Life Sciences and BYRD Health for a practical session to help you avoid last-minute surprises and set your organization up for long-term regulatory success. 📅 Thursday, June 5 🕛 12 PM ET / 9 AM PT This session will cover: ✅ Key UDI pitfalls and how to avoid costly data and system errors ✅ Best practices for validated, tech-enabled quality management ✅ Strategies for aligning UDI data across EUDAMED, GUDID, and more 👉 Register today: https://bit.ly/434ux59 #MedicalDevices #EUDAMED #LifeSciences #UDI

🤖 AI isn't just the future of life sciences—it's already reshaping it. Predictive analytics powered by AI and machine learning is helping life sciences organizations accelerate R&D, optimize operations, and anticipate market shifts before they happen. In our latest blog, we explore how forward-thinking teams are using AI to: ✅ Speed up drug discovery and trial design ✅ Streamline supply chain and manufacturing workflows ✅ Reduce equipment downtime with predictive maintenance 🔗 Read the blog: https://bit.ly/3F2XKFw #LifeSciences #PredictiveAnalytics #AI #MachineLearning #DrugDevelopment #DigitalTransformation #Pharma #Biotech #USDM

We’re thrilled to celebrate our very own John Zhang who was featured at ServiceNow Knowledge 2025! As a 3-time ServiceNow MVP, John’s leadership, expertise, and passion for innovation continue to inspire the ServiceNow community and beyond. His contributions not only elevate USDM Life Sciences but also drive meaningful transformation in the life sciences industry.   👏 Congratulations, John, on this well-deserved recognition! We’re proud to have you representing USDM on such a global stage. #USDM #LifeSciences #ServiceNow #Innovation 

Life sciences labs are increasingly targeted by attackers—yet many still rely on outdated infrastructure not built for today’s threats. In our latest blog, we look at how Offensive Security Testing goes beyond traditional pen testing to expose real vulnerabilities in lab environments. Learn how organizations are: 🔍 Identifying weak spots before attackers do 🔐 Securing sensitive research and IP 🧱 Strengthening defenses with Zero Trust and microsegmentation 🔗 Read the blog: https://bit.ly/3GMn1Vh #LifeSciences #Cybersecurity #DataSecurity #USDM

In highly regulated environments like life sciences, traditional GxP training methods often fall short—especially when the stakes include product quality, patient safety, and regulatory compliance. Modern organizations are rethinking their approach with technologies like: 🧠 AI for personalized learning pathways 🧬 VR and AR for immersive, hands-on training 🔒 Blockchain for secure, auditable training records In our latest blog, we explore how advanced tools are transforming GxP training—from a compliance necessity into a strategic advantage. If you're aiming to reduce risk, boost ROI, and prepare your teams for whatever comes next, this one’s for you. 🔗 Read the blog:https://bit.ly/4feRRS9 #LifeSciences #GxP #AI #VR #USDM

Congratulations to USDM’s Jay Crowley for contributing to the newly released Fundamentals of Medical Device Regulations: A Global Perspective, published by the Regulatory Affairs Professionals Society (RAPS). This guide—shaped by the insights of over 75 global experts—is designed to help regulatory professionals around the world navigate the evolving landscape of medical device regulations. As Vice President of Medical Device Solutions and Services at USDM, Jay brings deep expertise in Unique Device Identification (UDI) and global regulatory strategy. His contribution reflects the kind of deep expertise USDM brings to life sciences companies navigating complex regulatory challenges. 📘 Learn more about the guide here: https://hubs.la/Q03kJnvn0 #USDM #LifeSciences #RAPS

In life sciences, where patient safety and data integrity are non-negotiable, managing third-party risk isn’t just a checkbox — it’s critical. From cybersecurity threats to evolving regulatory frameworks, vendor oversight is getting more complex. That’s why organizations are turning to more automated, insight-driven approaches to risk management. ✅ In our latest blog, we explore: ✅How to proactively manage risk across your vendor ecosystem ✅Why real-time monitoring matters more than ever ✅Ways to strengthen compliance without slowing down operations 👉 Read more: https://bit.ly/43n8jgC #LifeSciences #Compliance #ThirdPartyRisk #Cybersecurity #TPRM #Biotech #MedTech #Pharma