KLIFO
Birgitte Friborg has extensive experience in quality management and clinical supply, currently serving as a Senior Clinical Supply Manager at KLIFO A/S since November 2021. Prior positions include roles as a Quality Specialist at Takeda Pharma A/S, Senior QA Specialist at Nomeco A/S, and QA GDP Compliance Manager at Takeda, where responsibilities encompassed quality oversight and compliance for distribution centers. Birgitte also held key positions at companies such as Alcon Nordic, where responsibilities involved managing the Nordic Quality Management System and leading audits. Educational qualifications include a degree in Laborant, Kemi from Laborantskolen i København.
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KLIFO
KLIFO is an integrated North-European drug development consultancy with significant experience in partnering with pharmaceutical and biotech companies. We enable our partners to maximise opportunity, mitigate risks, drive innovation and achieve efficient project advancement. We offer end to end solutions across all drug development areas, including strategic project management, regulatory affairs, clinical development, clinical trial supply, quality assurance (QA), Chemistry Manufacturing and Controls (CMC) development, non-clinical development and pharmacovigilance in relation to the development of pharmaceutical products. We provide strategic advice as well as operational support in all these areas, and we partner with clients on portfolio strategies, project development strategies and project execution. KLIFO has offices in Denmark, Sweden, Germany and The Netherlands and employs more than 150 highly skilled employees.