At Billev Pharma we are specialised in both human and veterinary pharmacovigilance. Billev Pharma has a pharmacovigilance system for both human and veterinary medicinal products. We are therefore able to assist clients who do not have a pharmacovigilance system of
Our regulatory team is growing and currently counts 15 regulatory specialists
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
We experience increasing demand for our regulatory services
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
Our RA team continues to grow
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
10 years anniversary
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
Promotion
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
Our RA team is growing and continues to in 2021…
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
Extension of our RA team with an experienced Regulatory CMC specialist
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 erfaren RA specialist – Stillingen er besat
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
Konsulenter i en Coronatid
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