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Karen Bryde Frisk
Director of Regulatory Affairs GN Hearing A/S
Karen Bryde Frisk is a professional in the medical device industry, currently serving as the Director of Regulatory Affairs at GN Hearing, a part of the GN Group.1 She has extensive experience in regulatory compliance and product quality management within the hearing aid sector.
Career at GN Hearing
Karen joined GN Hearing four years ago, in 2020.1 Throughout her tenure, she has held various positions within the company:
- Initially tasked with regulatory compliance responsibilities
- Served as Product Quality Manager for technologically advanced medical devices2
- Recently announced her return to the role of Director of Regulatory Affairs1
Expertise and Responsibilities
Karen's expertise lies in:
- Regulatory compliance: She has a strong background in this field, having "grown up" in the industry focusing on regulatory affairs.1
- Product quality management: She has experience overseeing quality for advanced medical devices.2
- Medical device technology: Karen works with innovative hearing aid products, such as the recently unveiled ReSound Nexia.3
Professional Milestones
- In June 2023, Karen celebrated her third year with GN Hearing, reflecting on her journey and growth within the company.4
- She has been involved in product launches, including the announcement of ReSound Nexia, a next-generation hearing aid designed to redefine user experience.3
Karen Bryde Frisk's LinkedIn profile (username: karen-bryde-frisk-1985974) showcases her professional journey and contributions to the hearing aid industry, particularly her roles within GN Hearing and her expertise in regulatory affairs and product quality management.