Trine Fabricius Holm has been with us for 2 years now working as a Regulatory Affairs Manager. Trine has more than 20 years of experience with national and European procedures, referrals and regulatory strategies among others from the Danish Medicines
Top-notch medical translation is our thing!
Make sure to let us handle your translations – that is, if you want to save time and money without compromising quality. High-quality translations make your way through the marketing authorisation process so much smoother. Let our team of trained
Let us handle your medical translations!
Medical translation requires a mastery and knowledge of the medical field. The specific terminology and compliance with the current regulation is unique to the industry – something we specialize in. It’s important that your translations are entrusted to a professional
Vi søger fortsat en specialist til vores pharmacovigilance team – Stilling er besat
Er du udadvendt og sætter du høje standarder for dig faglighed, så kan du læse mere om stillingen her:
Vi søger erfaren Pharmacovigilance Specialist – Stilling er besat
Vi mangler en erfaren medarbejder til vores pharmacovigilance team. Er du den kollega vi leder efter? Ved du en masse om pharmacovigilance? Kunne du tænke dig at arbejde i et uformelt og fagligt miljø med kompetente kollegaer? Er du engageret
Vi søger studentermedhjælpere til vores pharmacovigilance team – Stilling er besat
Billev Pharma søger studerende, der er færdig med bachelordelen og som er nysgerrige efter at lære mere om bivirkningsovervågning af lægemidler og kunne tænke sig, at hjælpe os med de daglige opgaver. De daglige opgaver vil bestå af: Ugentlige litteratursøgninger.
Pharmacovigilance
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