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Use Patient Population Data to Improve Therapy Lifecycle Decisions

3 Dec 2026·Canada

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Pharmaceuticals

Use Patient Population Data to Improve Therapy Lifecycle Decisions

Finding the Right Patients Doesn’t End With Trial Enrollment. Register to Stay Ahead.

  • Date

    3 December 2026

  • Location

    Toronto, Canada

  • Event Type

    Webinars

  • Delivery Format

    Virtual Only (Online)

Register for Free
Use Patient Population Data to Improve Therapy Lifecycle Decisions logo

Understanding who the right patients are and how to find them remains a challenge across the therapy lifecycle. From clinical development and trial enrollment through post-approval, each stage generates new insights into patient populations, disease characteristics, diagnostic and healthcare journeys. This webinar explores how integrated patient data can improve patient identification and inform decisions throughout the therapy lifecycle.

This webinar brings together industry experts to examine how genomic, phenotypic, claims and electronic health record (EHR) data can help identify and better understand rare disease patient populations across the therapy lifecycle. The discussion will highlight how real-world data can identify patients who may otherwise be overlooked, support clinical development and provide insights that inform future therapeutic development programs.

The featured speakers will also explore how these insights can be applied across the therapy lifecycle, drawing on large-scale, clinically derived genomic datasets containing millions of genetic tests, exome and genome sequences and phenotypic data points, complemented by claims data. Integrating these complementary data sources can strengthen the understanding of patient populations, reveal patterns in healthcare journey and support evidence-based decisions from discovery through post-approval.

Register for this webinar to learn how genomic and real-world data can improve patient population identification, support clinical development and generate insights that inform future therapeutic programs.

Who Should Attend

This webinar will appeal to professionals working in rare disease research, genomic medicine, clinical development, commercial strategy and real-world evidence, including:

  • Research Scientists and Genomic Scientists

  • Molecular Geneticists and Epidemiologists

  • Translational Scientists and Biomarker Researchers

  • Clinical Development/Operations

  • Precision Medicine

  • Commercial Strategy and Market Access professionals

  • Medical Affairs Directors and Medical Science Liaisons

  • Real-World Evidence (RWE) and HEOR professionals

  • Bioinformatics Scientists and Clinical Data Scientists

Register free on Xtalks: https://xtalks.com/webinars/use-patient-population-data-to-improve-therapy-lifecycle-decisions/

Learning Outcomes

Attendees will:

  • Explore the challenges of identifying and reaching rare disease patient populations throughout clinical development and commercialization

  • See how genomic, phenotypic, claims and EHR data can uncover patients, disease characteristics and healthcare journeys

  • Understand how patient-level insights can support cohort identification, clinical trial enrollment and clinical development decisions

Pricing & Registration

Attendance Fee

Free

No registration fee

Register for Free

Pricing & Registration

Attendance Fee

Free

No registration fee

Register for Free

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Speakers

Hear from world-class voices shaping Pharmaceuticals.

  • Colleen Caleshu, MSc, LCGC

    Colleen Caleshu, MSc, LCGC

    Senior Director of Translational Research

    GeneDx

  • Joe Walter, MBA

    Joe Walter, MBA

    Senior Director of Marketing

    Neurvati

  • Sarah Chang, PhD

    Sarah Chang, PhD

    Medical Strategy Lead

    UCB

Event Location & Venue

Join us at this world-class venue designed to inspire meaningful connections.

Location

Toronto, Canada

Date & Time

3 December 2026

14:00 – 15:00

Timezone

UTC-05:00 (EST - Eastern Standard Time)

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Xtalks logo

Organized by

Xtalks

Corporate (Internal Event Organiser)

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