02.02.2024
Sanna Hosio appointed as Quality and Regulatory Affairs Director
We are happy to announce that Sanna Hosio has been promoted to the position of Quality and Regulatory Affairs Director of Cerenion. With this new appointment, she will also assume the role of Person Responsible for Regulatory Compliance (PRRC), as defined in the Medical Device Regulation (EU) 2017/745 and continue her work as a member of the management team.
Sanna has been working for Cerenion for 3 years, and during this time she has advanced from specialist to the head of the quality team and a member of the management team. She has done amazing work to develop our quality management system to meet the requirements of the medical device industry and the company's strategy. As a person, Sanna is well organized and makes sure that all relevant requirements are adopted and applied, and at the same time she’s a true enabler. We’re happy to have her onboard!
As the PRRC, Sanna ensures the compliance of released devices and technical documentation, as well as the post-market surveillance (PMS) and vigilance activities concerning those devices. "I have been given a brilliant opportunity to gain experience and knowledge. In this role, I will continue to work towards our goals for enhancing the EEG monitoring", Sanna says.
Highlights
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