Building Breakthroughs: How Research-Ready Data Transforms Clinical Development

Biotech, Life Science, Pharma,
  • Tuesday, June 03, 2025 | 10:30am EDT (NA) / 3:30pm BST (UK) / 4:30pm CEST (EU-Central)
  • 60 min

The path to groundbreaking discoveries in clinical research starts with a single, vital element: trusted data.

But, how can you be sure that the data fueling your research is accurate, comprehensive and ready for exploration? In a rapidly evolving landscape of medical research, the ability to access clean, reliable and research-ready data can mean the difference between a stalled study and a breakthrough discovery.

In this webinar, the expert speaker will dive into the science of data integrity and how the frontiers of research-ready data are expanding across new domains and global regions. He will guide you through the rigorous journey of clinical data—from ingestion to harmonization—ensuring that it meets the highest quality standards before it ever reaches your hands. This webinar will explore:

  • The science behind data integrity—why it matters and how it impacts clinical research outcomes
  • How data integrity is ensured while expanding data availability both in breadth across regions and depth across clinical domains
  • The unseen challenges of data curation and how common issues can be solved before researchers even access the data, allowing them to focus on discovery rather than cleaning

Whether a clinical analyst, biostatistician or part of a healthcare organization looking to contribute research-grade data, this webinar will show how trusted data can unlock new possibilities for clinical trials and drug development.

Register for this webinar to learn how data integrity, accessibility and readiness can drive real breakthroughs in clinical trials and drug development.

Speaker

Matvey Palchuk, TriNetX

Dr. Matvey Palchuk, MD, MS, Chief Medical Informatics Officer, TriNetX

Dr. Matvey Palchuk, MD, MS, FAMIA is an expert in clinical informatics, semantic interoperability and data quality with extensive experience in healthcare information management, data acquisition and interoperability, the design of user interfaces for point-of-care applications, information modeling, knowledge management and quality measure reporting.

Message Presenter

Who Should Attend?

This webinar will appeal to experts in data integrity and clinical research that ensures accurate, compliant and high-quality clinical trial data, supporting regulatory compliance, patient safety and data-driven drug development.

  • Clinical Data Manager
  • Data Integrity Specialist
  • Clinical Research Associate (CRA)
  • Regulatory Affairs Manager
  • Quality Assurance (QA) Auditor – GCP Compliance
  • Clinical Data Scientist/Clinical Trials Data Analyst
  • GCP Compliance Manager
  • Pharmacovigilance Data Manager
  • Biostatistician

What You Will Learn

Attendees will learn about:

  • How data integrity directly impacts research outcomes
  • What it takes to ensure data is truly research-ready
  • How expanding access across regions and clinical domains can unlock new opportunities for clinical trials and drug development

Xtalks Partner

TriNetX 

TriNetX is a global network of healthcare organizations and life sciences companies driving real-world research to accelerate the development of new therapies. Through its self-service, HIPAA, GDPR, and LGPD-compliant platform of federated EHR, datasets, and consulting partnerships, TriNetX puts the power of real-world data into the hands of its worldwide community to improve protocol design, streamline trial operations, refine safety signals, and enrich real-world evidence generation.

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