How to Leverage Real World Data to Achieve Faster Insights for Better Adverse Event Detection and Reporting

Commercialization and HEOR, Drug Safety, Life Sciences, Medical Device, Medical Device Safety and Regulation, Pharmaceutical, Pharmaceutical Regulation ,
  • Wednesday, January 16, 2019 | 11am EST (NA) / 4pm GMT (UK) / 5pm CET (EU-Central)
  • 60 min

Pharmacovigilance data is growing everyday as organizations seek to drive adverse event detection and reporting with more data, real time data, and published literature. As the volume of this data continues to grow, it becomes increasingly difficult to operationalize it. Harmonizing, semantic enrichment, and making searchable all of the available data is the first step to detecting relevant signals and exposing critical insights.

This presentation outlines the challenges of using real world data for pharmacovigilance, and the implications of current inefficient data search and integration capabilities. Featured speakers will discuss how a next generation semantic operational data hub can advance all aspects of pharmacovigilance and increase your organization’s ability to adapt to a changing regulatory landscape.

Join this webinar discussion to learn:

  • How traditional data architectures limit adverse event reporting and compliance
  • How semantic databases can bring context and meaning to diverse data sets
  • How a metadata catalogue can deliver immediate insights by delivering relevant search results

Speakers

Bill Fox, Chief Strategy Officer, Healthcare and Life Sciences, MarkLogic

Bill Fox, JD MA, is Global CSO of Healthcare and Life Sciences at MarkLogic. Bill is known as a nationally recognized healthcare, life sciences, insurance, data strategy and analytics business leader. A former State and Federal prosecutor, law firm partner, consultant and technology executive, he has established a reputation as a leading voice on issues related to healthcare analytics, big data, payment integrity, data security, compliance, strategy and risk.

Message Presenter

Imran Chaudri, Chief Architect, Healthcare & Life Sciences, MarkLogic

Coming soon…

Message Presenter

Who Should Attend?

Senior professionals from biopharmaceutical and medical device companies involved in:

  • Data Analytics/Bioinformatics
  • Drug Safety/Pharmacovigilance
  • Epidemiology
  • Health Economics & Outcomes Research (HEOR)
  • Market Access
  • Regulatory Affairs
  • Scientific Affairs
  • Data Architecture/Solutions Architecture/Enterprise ArchitectureBrand Management
  • Brand Management

What You Will Learn

  • How traditional data architectures limit adverse event reporting and compliance
  • How semantic databases can bring context and meaning to diverse data sets
  • How a metadata catalogue can deliver immediate insights by delivering relevant search results

Xtalks Partner

MarkLogic

As the world’s best database for integrating data from silos, MarkLogic’s database platform empowers our customers to be more agile and cost efficient, advancing development and delivery of RWE to expedite pre- and post-regulatory approval processes. Life Sciences organizations trust MarkLogic to help accelerate the development and availability of new drug therapies and medical devices.

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