Medical and Regulatory Affairs Consultancy
Corona betød en stor omvæltning for manges arbejdsliv. Men ikke for vores, for vi fortsatte bare det, som vi havde gjort siden vi overtog Billev Pharma i 2015, men nu i meget højere grad. Vores medarbejdere havde i forvejen mulighed
As of January 2020, Susanne Thiilborg and Bo Kreilgaard will hold the position of Senior Regulatory Affairs Manager and Lisbeth Bonde Jensen now holds the position of Senior Pharmacovigilance Manager. Lisbeth is also QPPV for one of our major accounts.
Vi søger en erfaren Regulatory Affairs Manager, som hurtigt vil kunne arbejde selvstændigt med opgaverne. Ved du en masse om CTD, eCTD og mere specifikt om et eller flere af modulerne 1-3? Du skal indgå i et team med dygtige
As of January 2020, Karen Jensen will hold the position as Head of Regulatory Affairs and Charlotte Munk Ejlersen now holds the position as Senior Regulatory Affairs Manager. Karen and Charlotte, together with the rest of our regulatory team, achieve
29-31 January we are attending first the Pharmacovigilance Conference and then the Regulatory Affairs Conference arranged by Medicines for Europe at the Hilton Hotel, Amsterdam.
Maria Brogaard is our state-authorised translator who has been with us for more than 15 years. Maria provides high-standard translations and proofreading of product information and all other documents in connection with regulatory procedures and pharmacovigilance in an environment where
In February 2019 Susanne Thiilborg, Ph.D.Pharm., began a position as Regulatory Affairs Manager with Billev Pharma. Susanne has more than 20 years’ experience within analytical chemistry from the pharmaceutical company Lundbeck. Susanne accounts for all possibilities and reviews the relevant
We are happy to announce the promotion of Charlotte Lindorf Eriksen and Sana Iqbal from Officer to the position of Manager. Charlotte and Sana have been with us for 4 years and have both shown an impressive ability to upskill
Trine Lorentzen, M.Sc. Pharm., filled the recently established post as QA Manager. Trine has several years of solid experience with Good Distribution Practice (GDP) and the function as Responsible Person. Are you facing an inspection? Are you struggling to keep
In June 2018 Karen Jensen, M.Sc. Pharm., joined our regulatory team. Karen and our regulatory team can assist you with both European and national initial MAAs or maintenance activities. Karen is a generous co-worker and has more than 16 years