Clinical & Regulatory Affairs Expert
Jasmin brings 7 years of experience writing clinical evaluations, as well as, leading the quality system aspects of design controls, risk management, usability, and post-market surveillance for class IIa devices. Having a unique dual role as both a product manager and regulatory professional, she was able to streamline customer and regulatory requirements into the product development process.
Jasmin about working at Qserve:
"I first discovered Qserve when I was searching for webinars on the MEDEV 2.7/1 Rev 4 requirements. I had attended many regulatory training and webinars over the years, but I was struck by the approach that Qserve used in teaching. It was obvious that the consultants are not only knowledgeable, they also enjoy what they do, and work hard to make sure their clients get what they need. I am proud to be part of the Qserve team."
Before transitioning into the regulatory aspects of medical device development, she worked in the pre-clinical research sector developing reagents to study disease progression and treatment progress in lung cancer and various hematological malignancies. Jasmin has a BSc degree in Microbiology from the University of New Hampshire. Over the years, she developed a special interest for technical writing in which she took specialized courses and developed her skills in medical writing. This has given Jasmin a broad basis technically and in the regulatory and clinical field.
Learn more about our services within Regulatory Affairs & Clinical Affairs.