Skip to Main Content

Get in touch with our Clinical Research & Trials team.

Kate L. Bechen

Team Lead
View our entire team  Download Service 
Capabilities /

Clinical Research & Trials

Focused on keeping clients on track.

To make it to market, new drugs and medical devices must first undergo clinical research and trials. Husch Blackwell negotiates the often complicated contracts that frame  these trials. We advise clients on drafting informed consents that meet all regulatory requirements, as well as on interactions with institutional review boards concerning protocols and study monitoring.

For trials supported by the National Institutes of Health or other government agencies or grants, we carefully craft the proper trial documentation to ensure regulatory compliance, protect intellectual property interests and minimize business liability exposure.

Related areas of focus:

Get in touch with our Clinical Research & Trials team.

Kate L. Bechen

Team Lead
View our entire team  Download Service 
Testimonial Tina Guilder, CEO, Virtus Pharmaceuticals

“The Husch Blackwell attorneys were fierce and tireless advocates for Virtus. In the face of aggressive actions by our competitors and FDA regulators, they developed and executed a legal plan that protected an important market for us. They have my gratitude and highest recommendation.”

Read how invested partnerships make a difference
Client Results

Husch Blackwell's seasoned team leads clients forward.

See examples from previous projects