On-demand webinar:

Create safer, better Oncology trial outcomes with real-world data

In this webinar, you’ll learn how incorporating real-world data into your clinical trial system can help you:

  • Craft trial protocols and study designs around data, making them more efficient
  • Improve the quality of evidence generated by your trial
  • Ensure trial continuation is safe and effective for patients' long-term
  • Reduce patient and site burden

Watch on demand

Clinical Trials with Real-World Data

Health data fragmentation is a hurdle for oncology clinical trials. With clinical trials being one of the most vital sources of evidence on drug effectiveness and safety in oncology clinical trials, bridging the gap between clinical trial data and real-world data (RWD) is imperative. 
Our speakers:

SVP, DCT Solutions, Oncology at Medable

A scientist by training, Vera holds a BA in Biochemistry from Harvard College, a PhD in Cell and Molecular Biology from the Penn Med.

Michelle Hoiseth has been working in the drug and device development industry for 30 years.

MaryAnne Rizk is a Chief Strategy Officer at Medable.

Clinical Trials with Real-World Data

Health data fragmentation is a hurdle for oncology clinical trials. With clinical trials being one of the most vital sources of evidence on drug effectiveness and safety in oncology clinical trials, bridging the gap between clinical trial data and real-world data (RWD) is imperative. 
Our speakers:

SVP, DCT Solutions, Oncology at Medable

A scientist by training, Vera holds a BA in Biochemistry from Harvard College, a PhD in Cell and Molecular Biology from the Penn Med.

Michelle Hoiseth has been working in the drug and device development industry for 30 years.

MaryAnne Rizk is a Chief Strategy Officer at Medable.