Ready to see what’s next for Medical Information? Join our live webinar on Voice Intake for IRMS MAX and discover how AI-powered voice revolutionizes IRMS cases. Still time to register:
https://t.co/Qw6nsa7xce
Medical Information teams: join us May 28 at 11:00 AM ET to see how IRMS MAX and Savio Labs bring AI-powered voice-to-case intake, approved-content matching, multilingual capture, and audit-ready compliance together. Register: https://t.co/XCGD6npTI0
As MAPS EMEA continues in Zurich, catch up with Greg Davies and Mathis Renier to learn what IRMS MAX and Savio Labs can do for faster intake and smarter case handling.
Book a demo: https://t.co/iQBkfMpqt2
#MedicalAffairs#MedicalInformation#MAPSEMEA#IRMSMAX
MAPS EMEA starts this Sunday in Zurich. @Anju Software will be there with Greg Davies and Mathis from Savio Labs to discuss stronger MedInfo workflows, connected publication planning, and real operational value. Attending MAPS? Book time with us.
#MedicalAffairs#MAPSEMEA
Discover how cleaner call capture, stronger triage, and structured case creation can work. Join Anju Software x Savio Labs for a webinar on Voice Intake for IRMS MAX.
📅 May 28, 2026 | ⏰ 11:00 AM ET
Save the date.
#MedicalAffairs#MedicalInformation#IRMSMAX
If you work in medical affairs, you already know: Intake. Triage. Routing. Drafting. MLR. Approval. Delivery. Tracking. Insight capture. The workflow must be operational. Explore more: https://t.co/0eKqqnFFHB
#MedicalAffairs#MedicalInformation#MedicalPublication#LifeSciences
That's a wrap on #ISMPP2026. Thank you to everyone who visited Anju at Booth 9, joined a demo, asked thoughtful questions, and explored what's next for publication planning and scientific communications. The momentum continues here: https://t.co/KbOht3ztwZ
#MedComms#MedPub
If study startup delays, manual builds, or resource bottlenecks have held your team back, you can’t miss this.
Live Webinar
𝗡𝗼𝘃𝗲𝗺𝗯𝗲𝗿 𝟮𝟬, 𝟮𝟬𝟮𝟱
𝟭𝟬:𝟬𝟬–𝟭𝟭:𝟬𝟬 𝗔𝗠 𝗘𝗦𝗧
🔗 Register now before seats close: https://t.co/jLKPSrgqUD
#clinicaltrials#aiclinical
In our world of eClinical and medical intelligence, the question is: how do we prove the long-term ROI (cost, compliance, patient benefit) of systems now considered “bleeding edge”?
**How is your team thinking about ROI when making digital investments?
We spend a lot of time talking about AI as if it’s the destination.
But in clinical research, AI is most powerful at the start — when it helps us ask the 𝗿𝗶𝗴𝗵𝘁 questions:
What upstream question is your team trying to answer better?
That’s a wrap on DIA Med Info 2025!
Thank you to everyone who joined us in London to share ideas and explore new ways technology can elevate Medical Affairs and Medical Information practices.
#DIAMedInfo#MedicalAffairs#LifeSciences#AnjuSoftware
See you at DIA Med Info 2025!
We’re bringing together innovation and expertise to help Medical Affairs teams deliver accurate, compliant, and insight-driven information faster than ever.
Meet our team at booth #7 in London!
We’re honored to have been awarded Best of Show at SCOPE Europe 2025 in Barcelona!
Our team continues to push the boundaries of what’s possible in clinical research technology by delivering innovation that drives efficiency, collaboration, and impact across the life sciences.
Day 1 at #SCOPE2025! Excited to meet so many innovators shaping the future of clinical trials and medical data.
Stop by the booth #48 to explore how Luminee, TrialMaster, and TA Scan help streamline workflows, enhance data quality, and unlock actionable insights.
In clinical research, the difference between insight and overload is how you see the data.
Join Elke Ydens at #SCOPE2025 at booth #48 to discover how TA Scan helps you accelerate feasibility, optimize site selection, and identify the right experts worldwide.
Clinical research has come a long way in helping patients with arthritis 𝘣𝘶𝘵 recruitment, retention, and equitable access still lag.
Every study design is a chance to reduce friction — and build something that meets patients where they are.
Clinical research shouldn’t move at yesterday’s speed.
Join Tim Lyons at #SCOPE2025 as he shares how Luminee accelerates study startup and protocol design without compromising quality or compliance.
🚀 Visit Booth 48 to see Luminee in action.
🔗 https://t.co/IucYSj9RZL
This Health Literacy Month, we’re reminded that accessible, timely, and patient-centric information isn’t just a public health issue — it’s a design challenge in clinical trials, too.
💡 How is your team prioritizing health literacy in study design or content delivery?
That’s a wrap on #SCDM2025!
We had a blast introducing Luminee and connecting with many forward-thinkers reshaping the future of clinical data.
If you didn’t get a chance to meet us onsite, let’s connect, we’d love to show you what’s next.
Let's talk: https://t.co/Yl9tBF95sg