RWE helps accelerate oncology drug development timelines by 1-3 years

  • Key insights from the research included: engage the FDA early to confirm appropriate data sources; select appropriate data sources to ensure real-world data are high quality and fit for purpose
  • “Moreover, we found that inclusion of RWE helped accelerate oncology drug development timelines by 1–3 years. That directly relates to getting urgently needed treatments into the hands of patients with difficult-to-treat cancers.“

Maral DerSakissian, Analysis Group Vice President

Click here to learn more.

About SVMPharma

SVMPharma is an innovative strategic consultancy, specialising in Real-World Evidence (RWE) for the pharmaceutical industry. SVMPharma generates RWE within UK and Europe through bespoke online Real-World Treatment Evaluators, leading to successful health technology appraisal (HTA) submissions. Clinical trial programmes do not reflect real-world clinical practice and outcomes, RWE supplements and enhances clinical datasets. SVMPharma’s specialist teams focus on delivering the outcomes that matter to your brand.

For more information, please visit and contact us at

ref: DEC2021BR002