Real-World Evidence Forum – Real-World Evidence Forum

Real-world evidence can provide key insights that will help drive down medical costs, as well as improve both product safety and effectiveness. Unfortunately, the relevance and validity of user-collected and practiced-based real-world data is a challenge within the clinical health industry. If real-world data isn’t properly analyzed it can be tricky to utilize successfully. Companies must have an in-depth understanding of the data landscape and how to assess real-world data sources, analytics and applications to build real-world data platforms.

Proving safety and effectiveness through a randomized clinical trial no longer secures the success and profitability of a drug or device. Companies must now demonstrate evidence of successful real-world outcomes to distinguish their products in an aggressive environment, while also fulfilling the requests of regulators, insurance companies, healthcare providers and patients.

The Real-World Evidence Forum, taking place on July 17-18, 2017 in Philadelphia, will bring together clinical health professionals to address how to operationalize the process of collecting real-world data. Our expert staff will discuss how to utilize real-world evidence to demonstrate both the clinical effectiveness and cost-effectiveness of your product. Attendees will gain a better understanding of how electronic data sources are changing the way real-world data is being collected. This conference will offer attendees insight into how real-world evidence will help decrease costs, define innovative outcomes and minimize the number of patients exposed to potentially harmful medications.

Keynote Speakers

 

Featured Speakers

Top Five Reasons to Attend

  1. Discuss how the industry is transforming the drug development process through the use of real-world evidence
  2. Learn to operationalize the process of collecting real-world data
  3. Use real-world evidence to demonstrate both the clinical effectiveness and cost-effectiveness of your product
  4. Discover how electronic data sources are changing the way real world data is being composed
  5. Examine the need for greater data sharing practices and transparency of methods when used for regulatory decision-making

Who Should Attend

This conference is ideal for life science professionals (pharma, biotech and medical device thought leaders; physicians; payers; academics) with responsibilities in the following areas:

  • Real-World Evidence
  • Phase IV
  • Postmarket Surveillance
  • Late Phase
  • Medical Affairs
  • Data Management
  • Project Management
  • Business Development
  • Clinical Development
  • Global Medical Affairs
  • Observational Research
  • HEOR/GHEOR
  • Patient Safety Surveillance
  • Clinical Trial Design and Management
  • Data Management Operational Support
  • Regulatory Affairs
  • Registry
  • Drug Safety
  • Patient-Reported Outcomes
  • Post-Approval

This event is also of interest to:

  • CROs
  • Clinical Trial Management Software Providers
  • Big Data Platforms