Author: Ulrikke Jensen

In May Mette Olsen, M.Sc. Pharm., joined our regulatory team. Mette has more than 10 years’ experience handling EU procedures. She also has experience with Pharmacovigilance and Marketing Compliance. Mette has vide experience working as a consultant. You can read

and our team working with preparation and review of analytical and pharmaceutical documentation is growing. In May Lone Pallesen, B.Sc. Ing. in chemistry joined our regulatory team. Lone holds a Diploma in Regulatory Affairs from Medicademy and has more than

In February Trine Fabricius Holm, M.Sc. Pharm., joined our regulatory team. Trine has more than 18 years of experience working as a Regulatory Project Manager from the Danish Medicines Agency. Trine has wide experience with national and European procedures. Trine

Our highly valued colleague Majbritt Eichmeier Hansen has been with us since March 2011 so this year we are celebrating her 10 years anniversary. Majbritt began her career in Regulatory Affairs, today she specialises in Pharmacovigilance. In 2015 Majbritt was

We are happy to announce the promotion of Katrine Schuster Ovesen from Officer to the position of Regulatory Affairs Manager.  Katrine has been with us for 6 years, starting as a student worker. She has shown an impressive ability to

Anne Ravnholdt Høcker joined Billev Pharma’s RA team in September. Anne has more than 20 years’ experience with writing and reviewing analytical and pharmaceutical documentation for MAAs and variations.  Anne had a strong wish to work part-time but at the

Karina Rebild joined Billev Pharma as a Regulatory CMC Specialist in August. With her more than 30 years’ experience – including sterile production and regulatory lifecycle management – she brings valuable knowledge to our RA team, which currently counts 15

Vi søger specialist til vores RA team, som hurtigt vil kunne arbejde selvstændigt med opgaverne. Har du flere års erfaring med registrering? Søger du nye udfordringer? Ved du en masse om vedligeholdelse af registreringer for humane lægemidler herunder udarbejdelse af

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.