Returning in person for its 10^th year anniversary, the IMPACCT: Real World Evidence Summit will deep dive into the use of RWE for regulatory submissions and improved clinical trial design to help you navigate the regulatory landscape.

Following recent FDA and EMA guidelines, this comprehensive industry-led forum will address how drug developers can leverage RWE from beginning to end of study, ensure clinical studies are well-designed, include appropriate protections for their patients and upload data integrity.

Join 100+ senior leaders in RWE, RWD, real world analytics experts & epidemiologists from pharma and biotech to take part in this three day summit with over 18 hours of exclusive content.

To know more visit: https://ter.li/tymfzh