Congratulations to BioTeknica principal Julie Larsen for her recent invitation and acceptance to join the FDAnews Medical Device Conference Advisory Board.
Julie Larsen, Principal, Director,
Inspection Readiness, BioTeknica
BioTeknica’s reputation as an expert regulatory compliance consulting firm has grown within the medical device industry due to the excellent work of its staff and in part to the continued marketing outreach and speaking engagements initiated by Julie. An expert speaker at many industry events, Julie has helped to identify important trends, provide counseling, and articulate key industry issues.
Most recently, FDAnews, a 40-year-old news media outlet that provides global and domestic regulatory, legislative, and business information for executives in industries regulated by the Food and Drug Administration, invited Julie to join its Medical Device Conference Advisory Board. The prestigious 12-member board is specifically dedicated to assisting FDAnews plan and develop its medical device conferences and webinars. The Board includes regulatory and quality affairs specialists, legal counsel, consultants, advocacy group representatives, and academics. Julie’s participation in this prestigious group will help grow awareness of BioTeknica within the industry.
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