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Billev Pharma ApS

Billev Pharma ApS

Medical and Regulatory Affairs Consultancy

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Uncategorized

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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

Ulrikke Jensen May 12, 2022May 12, 2022 Uncategorized No Comments Read more

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

Ulrikke Jensen June 28, 2021June 28, 2021 Uncategorized No Comments Read more

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

Ulrikke Jensen June 25, 2021June 25, 2021 Uncategorized No Comments Read more

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

Ulrikke Jensen March 26, 2021March 26, 2021 Uncategorized No Comments Read more

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

Ulrikke Jensen February 23, 2021February 23, 2021 Uncategorized No Comments Read more

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

Ulrikke Jensen February 1, 2021February 1, 2021 Uncategorized No Comments Read more

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

Ulrikke Jensen December 9, 2020December 9, 2020 Uncategorized No Comments Read more

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

Ulrikke Jensen November 20, 2020November 20, 2020 Uncategorized No Comments Read more

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

Ulrikke Jensen October 21, 2020January 21, 2021 Uncategorized No Comments Read more

Konsulenter i en Coronatid

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

Ulrikke Jensen June 12, 2020June 12, 2020 Uncategorized No Comments Read more
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