KLIFO
Helle Andersen is a seasoned quality assurance professional with extensive experience spanning several decades. Currently serving as a Senior QA Specialist at GCPKLIFOD since December 2024, Helle has previously held significant roles at ALK Abelló, including CQM Manager and Senior QA Compliance Manager from August 2008 to December 2024. Prior experience includes a position as Coordinating Manager QM-ITCyncron at Medicon A/S from November 1994 to July 2008, along with roles at Andersen Consulting (Accenture) and Danexpert a.m.b.a. as Secretary to the CEO. Helle Andersen studied at Copenhagen Business School, earning an ED in English from January 1976 to January 1977.
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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.