Register for the 14th IMPACCT Real-World Evidence Summit

Please select the appropriate price when booking. Bookings are subject to approval.

All prices are shown in USD.

Register by Friday, October 9 & Save up to $360

Drug Developer Pricing*

Full Access Pass

(Save $360)
Grants access to the Workshop Day & Full Conference

$4,037

On the Door: $4,397

Conference Only

(Save $180)

$2,919

On the Door: $3,099

Service Provider Pricing***

Full Access Pass

(Save $360)
Grants access to the Workshop Day & Full Conference

$5,037

On the Door: $5,397

Conference Only

(Save $180)

$3,719

On the Door: $3,899

* To be eligible for this price, the group or individuals must be from a biotech or pharma company that has a publicly available pipeline, and does not offer pay for services.

** To be eligible for this price, the group or individual must be full-time academic(s).

*** If you are a solution or service provider, have you considered sponsoring this event? Sponsorship includes multiple passes at a discounted rate. Inquire to learn more.

Prices exclude any applicable taxes. VAT or other indirect taxes may apply depending on event location and tax status. Eligible business customers may provide a valid VAT registration number at checkout where a reverse charge mechanism is available.

Unlock Group Discounts

Maximize value for money using special team discounts: Please note that discounts are only valid when three or more delegates from one company book and pay at the same time.

10% Off

When registering 2 attendees from one company

15% Off

When registering 3 attendees from one company

20% Off

When registering 4+ attendees from one company

Need Assistance?

If you have any questions about registration pricing, discounts or would like help in the booking process, contact us and one of the team will get back to you.

View The 2026 Event Guide

  • Explore 20+ real-world case studies across clinical development, regulatory, and market access 
  • Discover how leading pharma are embedding AI into RWE workflows 
  • Benchmark integrated evidence planning strategies across the lifecycle 
  • Identify solutions to improve data quality, access, and regulatory acceptance 
  • Share insights with cross-functional RWE, HEOR, and data leaders 
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