Clinical Affairs

Optimize your path to regulatory approval by leveraging our unparalleled
clinical affairs and development expertise.


Clinical Affairs Expertise

Bannick Primary understands the importance of timely, high-quality and cost-effective clinical development and our services help clients 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 help to ensure that your strategy will be sufficient to meet the requirements.

Together we can drive public health forward.

Our Clinical Study Services Include:

Clinical study design: premarket, safety, efficacy, postmarket

Protocol and CRF development

Clinical study management: investigator meetings, site training and monitoring

Statistical Analysis

Advise and guide your company on how to address and comply with the new EU Medical Device Regulation (MDR) requirements

Clinical Affairs
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