Drug development can be a lengthy and costly process, and it is believed that clinical trials make-up approximately 60% of these costs.  We understand the pressure sponsors are under to capture data quickly, safely and with the highest patient compliance rate possible and that is why we deliver ePRO expertise needed to support your drug development goals. The benefits we provide to sponsors include:

• Strategic Insight: Our experience and thorough understanding of drug development means that we don’t simply provide the technology for ePRO, but we partner with you to help you get quality results, faster.
  

• Advisory Board: We have assembled a team of respected and knowledgeable experts from the pharmaceutical industry to ensure that our processes and technology are applicable, usable and as relevant as possible to our users, both now and in the future.
  
  
• Innovative Technology: We bring ePRO innovations to market- first, harnessing and developing technology to improve the collection of data in clinical trials, capturing data quickly, accurately and with the highest possible patient compliance rate.
  
  
• Global Capabilities: We have extensive experience in all regions and extensive language capabilities, with our technology being used in 60 countries and 68 regional languages.
  
  
• Regulatory Expertise: We understand the tough regulatory requirements put on clinical trials. We work closely with the FDA to help develop industry guidelines of electronic PRO data in clinical trials.