Optimize your path to regulatory approval by leveraging our unparalleled
clinical affairs and development expertise.
Clinical Affairs Expertise
Optimize your path to regulatory approval by leveraging our unparalleled clinical affairs and development expertise. At Bannick, we understand the importance of timely, high-quality and cost-effective clinical development and our services ensure scientific integrity and compliance with applicable regulations and quality standards.
Your clinical evaluation is a critical element in any regulatory pathway. Our clinical experts can guide your company to compliance with FDA and the new EU Medical Device Regulations (MDR) requirements.
Together we can drive public health forward.
Our Clinical Study Services Include:
Clinical Study Strategy & Design
Post-market Clinical Follow-up
Protocol and CRF Development
Clinical Study Management
Investigator Meetings & Site Training
We are your subject matter experts!
We're Here To Help!
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