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Association for Clinical Data Management (ACDM25)

  • March 2-4, 2025 
  • Prague, Czech Republic
  • Booth #34 
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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:

1. 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.

2. Solutions Built for You 

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

3.  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 Real-Time Anomaly Detection 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. 

AI-Augmented CDM Roles: Driving Accelerated Data Review & Quality Management

March 4, 2025 | 10:40 AM - 11:25 AM CET

Presenter:

Rajesh Hagalwadi

Director, Clinical Data Solutions, MaxisIT Inc.

Description: Experience how AI is revolutionizing clinical data management with DTect AI, an advanced Agentic AI solution designed to accelerate data quality management across the clinical development lifecycle. This live showcase will demonstrate how AI-driven workflows and conversational AI Agents enhance data review speed, accuracy, and compliance, empowering teams to move beyond manual processes toward insight-driven, strategic decision-making.

See how AI identifies anomalies in real time, automates query generation, provides actionable recommendations, and ensures audit readiness with intelligent tracking of database modifications. Experience the future of clinical data management—faster reviews, greater accuracy, and seamless compliance, all powered by AI.

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.

Schedule to meet our experts at Association for Clinical Data Management
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Upcoming events

MaxisIT | PharmaSUG 2025, San Diego, CA

PharmaSUG US Conference 2025

MaxisIT at Outsourcing in Clinical Trials East Coast 2025

16th Annual Outsourcing in Clinical Trials East Coast 2025

MaxisIT at SCOPE 2025

Summit for Clinical Ops Executives (SCOPE 2025)

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 Luks

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 Data 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.

Schedule to meet our experts at Association for Clinical Data Management
[contact-form-7 id="3b04428" title="Events"]

Our Products

Clinical Trials Oversight System

Full data visibility and oversight by study and by portfolio.

Learn More

Data Management Workbench  

Full data visibility and oversight by study and by portfolio.

Learn More

Risk-Based Quality Management          

Full data visibility and oversight by study and by portfolio.

Learn More

Statistical Computing Environment          

Full data visibility and oversight by study and by portfolio.

Learn More

Clinical Data Repository        

Full data visibility and oversight by study and by portfolio.

Learn More

Software-Enabled Services    

Full data visibility and oversight by study and by portfolio.

Learn More

CTRenaissance® Clinical Data Analytics Platform

Full data visibility and oversight by study and by portfolio.

Learn More

Related Resources

Protocol Deviations in Clinical Trials: Why It’s Time for Smarter Oversight

Protocol Deviations in Clinical Trials: Why It’s Time for Smarter Oversight

AI-Enabled Risk-Based Monitoring: Enhanced Clinical Trial Oversight

3 Ways AI is Reshaping Business and How You Should Prepare for the Future

Value-Based Data: Real-World Comparison

Unlock Business Value from Clinical Data with an Outcomes-based Approach

The Advantages of AI for Risk-based Monitoring in Clinical Trials

Smarter Audit Trail Review: Agentic AI Strategies for Modern Data Managers

Agentic AI in Clinical Trials: From Hype to Real-World Implementation

4 Ways AI Transforms Clinical Operations: From Data Oversight to Risk Management

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Maxis AI delivers agentic AI-driven clinical trial data analytics, empowering life sciences teams with faster, smarter insights. With 3,300+ trials in cloud, our source-agnostic platform serves as a single source of truth. Backed by 20+ years of domain expertise, we simplify data management, accelerate timelines, and optimize outcomes across global clinical operations.