KLIFO
Sue Gregory is an experienced professional in the field of quality assurance and compliance, currently serving as the Director of GCP QA at KLIFO A/S since December 2020. Prior to this role, Sue Gregory was involved in GXP Compliance within R&D Operations at Savara from February 2020 to December 2020 and served as Clinical Compliance at Savara DK from January 2019 to February 2020. With a significant tenure at LEO Pharma from February 2010 to December 2018 as GCP QA, and previous experience as Associate Director of GCP Compliance at Genmab between March 2008 and February 2010, Sue Gregory developed a strong foundation in quality assurance during an earlier role at Lundbeck from 1998 to 2002.
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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.