Clare Rickel

Background

About Clare Rickel

As a Clinical Reports Specialist at BISCO since 2021, I specialize in the creation of Clinical Evaluation Reports, Post-Market Clinical Follow-Up Reports, and Periodic Safety Update Reports for class I and class II medical devices. My role is crucial in ensuring compliance with regulatory standards, particularly as I navigate the transition from the Medical Device Directive to the Medical Device Regulation. I am passionate about effective communication through writing, and I take pride in my ability to organize and plan complex documents efficiently. My dedication to time management allows me to meet tight deadlines while maintaining the highest quality standards. I hold a Regulatory Affairs Certificate in Medical Devices and am an active member of the Regulatory Affairs Professionals Society (RAPS) and the American Medical Writers Association (AMWA). These affiliations keep me updated on industry trends and best practices, further enhancing my expertise in regulatory writing.