Watch the Webinar On-Demand Now
Transforming Study Start Up to Reduce Site Burden

Clinical trials are more complex than ever. And 85% of them are delayed.

More screening criteria, expanded procedures, new vendor systems and tools, and increased data collection. So who bears the burden of all this progress? Sites.

Increased site burden means degraded performance, additional delays, and more problems for you. But it doesn't have to be that way.

Watch this webinar, as we discuss real clinical trial examples from emerging biotechs that will give you techniques to identify and mitigate risks sooner in your study, by:

  • Simplifying your approach to getting sites trained on your protocol and study documents - faster and with better results
  • Tailoring SIVs and remediation so every site you activate is ready to enroll - fast 
  • Reducing the amount of hours your teams spend on redundant and unnecessary work

Register to Watch On-Demand