We can work directly with your CROs and turn around requests for sponsor guidance and reviews in an expeditious manner. Our timely reviews will prevent you, the sponsor, from becoming the reason that your own timelines are not being met.


Ex-US Clinical Trial Agreements

Our attorneys can create a set of contracting parameters for your CRO’s use and will handle the escalation of certain matters, such as fair market value, use of study data, publication and indemnity on your clinical team’s behalf. Our knowledge of country-specific requirements in South America, the EU and Asia-Pacific will ensure a quick turn-around for any “sponsor-only” contract questions your CRO or clinical team may have. Furthermore, we can work directly with sites in Poland and Germany, as we have fluent attorneys on staff.