Webinar

Integrated Data Review (IDR): Accelerating Access to Quality Data in Clinical Trials

Join us for an insightful webinar on Integrated Data Review (IDR): Accelerating access to quality data in clinical trials. With ever increasing volume, complexity, and sources of clinical trials data, finding a single and comprehensive solution for data review is becoming a necessity. Integrated data review (IDR) offers an excellent solution for data review challenges faced by clinical operations, biometrics, and the medical monitoring teams.  By consolidating various data sources, IDR streamlines processes, improves data quality, and allows quicker access to data for actionable insights.  Discover how automation, standardized data formats and implementation of AI & ML, can help reduce cycle time and improve decision-making. Our experts will share benefits of IDR and real-world case studies, followed by a live demo of MaxisIT’s Data Management Workbench (DMW).

Key Aspects of the Webinar:

  1. Data review and data sources in clinical trials: Then and now
  2. Overcoming data silos: Build efficient data review processes to facilitate cross-functional collaboration
  3. Significance of Integrated Data Review (IDR): Learn how multi-level, unified data access helps reduce cycle time and helps with faster decision-making
  4. Data management techniques: Discover effective data collection, curation, and integration methods
  5. Key roles, interfaces, and stakeholders: Understand the importance of various team members in IDR
  6. Cutting-edge technology: Understand the role of AI, ML, and standardized data formats in optimizing data processing and quality
  7. Challenges and key takeaways
  8. Best practices and case studies: Gain insights from practical examples and expert recommendations
  9. Live demonstration of MaxisIT’s Data Management Workbench: Learn how DMW enables faster access to quality data via data integration and standardization
  10. Q&A session

Secure your spot now and don’t miss out on this opportunity to accelerate your clinical trials with cutting-edge data management insights!

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Speakers

Indrani Kakade is a distinguished leader with over 29 years of experience in Global Pharma and Outsourcing Industry. She is an early adopter of Clinical Data Management Outsourcing to India with experience in Study set up, Data Management , Statistical programming, Drug Safety & Pharmacovigilance/Drug Safety Operations. She has held leadership roles at Pfizer Pharmaceuticals, Cognizant Technology Solutions, Sciformix Technologies, and Cliantha Research.
She is known for her entrepreneurial skills in establishing and managing global operations and teams, having successfully led numerous large-scale projects and clinical study transitions across multiple geographies.
Currently works as an independent consultant for pharma, CROs and technology companies in the area of data management and analytics leveraging automation, AI and ML concepts.

With over 20 years of comprehensive experience, Greeshma Mundayat’s journey began with bedside patient consulting, evolving into a profound impact on patients’ trajectories and outcomes within clinical trials through innovative technology utilization. Proficient in Healthcare Management, Healthcare, Data Analysis, and Strategic Planning, Greeshma has exhibited her prowess in shaping the clinical data industry. Notably, her tenure at MaxisIT showcased her adeptness in revolutionizing approaches, driving strategic initiatives, and enhancing patient experiences within clinical trials through her visionary insights and technological implementations.

Indrani Kakade is a distinguished leader with over 29 years of experience in Global Pharma and Outsourcing Industry. She is an early adopter of Clinical Data Management Outsourcing to India with experience in Study set up, Data Management , Statistical programming, Drug Safety & Pharmacovigilance/Drug Safety Operations. She has held leadership roles at Pfizer Pharmaceuticals, Cognizant Technology Solutions, Sciformix Technologies, and Cliantha Research.
She is known for her entrepreneurial skills in establishing and managing global operations and teams, having successfully led numerous large-scale projects and clinical study transitions across multiple geographies.
Currently works as an independent consultant for pharma, CROs and technology companies in the area of data management and analytics leveraging automation, AI and ML concepts.

With over 20 years of comprehensive experience, Greeshma Mundayat’s journey began with bedside patient consulting, evolving into a profound impact on patients’ trajectories and outcomes within clinical trials through innovative technology utilization. Proficient in Healthcare Management, Healthcare, Data Analysis, and Strategic Planning, Greeshma has exhibited her prowess in shaping the clinical data industry. Notably, her tenure at MaxisIT showcased her adeptness in revolutionizing approaches, driving strategic initiatives, and enhancing patient experiences within clinical trials through her visionary insights and technological implementations.

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