[Webinar] Transforming Study Start Up to Reduce Site Burden

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

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

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

Join this webinar, as we discuss real clinical trial examples from emerging biotechs that will give you techniques to:

• Simplify your approach to getting sites trained on your protocol and SOPs - earlier and with better results
• Tailor SIVs and remediation so every site you activate is ready to enroll - fast 
• Reduce the amount of hours you, your CRO, and your team spend on redundant and unnecessary work