Association for Clinical Data Management (ACDM25)

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Join Us at ACDM 2025 to Discover Smarter Solutions for Integrated Data Review and Decision-Making 

Clinical trial data management isn’t just challenging—it’s complex and relentless. From juggling diverse datasets to ensuring compliance and streamlining workflows, the pressure to deliver results is constant. MaxisIT’s AI-powered solutions, driven by innovations like DTect AI, tackle these challenges head-on—optimizing review processes, identifying discrepancies, and enabling confident, data-driven decisions for seamless, efficient trial management.

Your Must-Visit MaxisIT Booth #34 at ACDM 2025: 

Experience Innovation Live :

  • Watch DTect AI transform fragmented data into clear insights in real-time.
  • Test-drive our platform with your own trial scenarios and and see AI reduce review times from weeks to hours. 

Solutions Built for You: 

  • Get personalized workflows matched to your trial complexity.
  • Discover how leading pharma companies cut costs by 40% using our platform.

Connect with Solution Implementation Leaders 

  • Deep-dive into success stories from Phase I-IV trials.
  • Get 1-on-1 consultation with our Clinical Data Workflow automation experts and learn best practices from successful implementations.  

What We’re Showcasing: 

1. Data Integration Framework :

  • Data ingestion seamlessly integrates clinical trial data from EDC, DCTs, CTMS, and other sources. 
  • Provides a unified view for efficient data management, superior data integrity, and actionable insights.

2. Data Management Workbench:  

  • Centralizes workflows to ingest data from diverse datasets, ensuring accuracy and reducing manual effort. 
  • Delivers sophisticated actionable insights for trial optimization, going beyond traditional dashboards. 

 3. AI-Enabled Data Validation with DTect AI

  • Automatically DTect data outliers and inconsistencies in real-time, ensuring enhanced accuracy and faster reviews. 
  • Integrates datasets and automates anomaly detection, transforming data validation into a strategic advantage. 

 4. Risk-Based Quality Management (RBQM)

  • Leverages AI-powered analytics to proactively identify and mitigate risks in clinical trials. 
  • Monitors QTL performance through adaptive analytics, ensuring compliance and enhancing trial outcomes.  

 5. Clinical Data Repository (CDR)

  • Streamlines data ingestion and aggregation, enabling high-quality workflows with early access to critical datasets. 
  • Reduces cycle times by automating data integration and minimizing manual effort. 

Connect with Us:

Swing by booth #34 to see how MaxisIT is transforming clinical data management journey. From smarter workflows to faster decisions, our AI-powered solutions are here to help you overcome challenges, enhance data quality, and supercharge your clinical trials.

Let’s book your personalized demo now at the conference.
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Meet Our Experts:

Nicole Powell

Senior Vice President

Nicole, a strategic leader with over 17 years of experience in the clinical research industry, has consistently driven transformative revenue growth across diverse markets. Her expertise lies in building strong partnerships and steering corporate strategies that align with evolving industry needs. At MaxisIT, Nicole is excited to bring her insights and passion for collaboration to expand the reach of MaxisIT’s Clinical Data Analytics Platform, helping clients streamline trials and achieve their objectives. Nicole recently led business development and marketing at SDC, where she pioneered growth initiatives and contributed to shaping the future of clinical trial technology. An experienced speaker, Nicole has presented at numerous industry conferences on tech-driven innovation in clinical research. She holds a BA from the University of Texas San Antonio and an MBA from Baylor University. Based in Virginia, Nicole enjoys golfing, exploring new destinations, and karaoke in her free time.

Jameson Luke

Senior Director

Jameson Luks boasts over 15 years of expertise with industry leaders like Cytel in clinical trial design and statistical products and now with MaxisIT in clinical data analytics. His deep insights and innovative approach consistently address the most pressing challenges for companies in the clinical trial landscape

Rajesh Hagalwadi

Director of Clinical Solutions

Rajesh is a PMP- and CSM-certified professional who brings over 15 years of experience implementing eClinical systems within the life sciences industry. His expertise includes pre-sales engineering, product advocacy, solution implementation, computer system validation (CSV), and end-user training. He frequently collaborates with account executives to develop strategic account plans, conduct client discovery, and deliver impactful presentations that showcase the technological and business value of MaxisIT.

Let’s book your personalized demo now at the conference.
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