Anja van Arkens
M.Sc.Pharm., Director & Owner
Ulrikke Lynge Jensen
M.Sc.Pharm., Director & Owner
Maria Brogaard
Authorised Translator & Regulatory Affairs Officer
Charlotte Munk Ejlersen
M.Sc.Pharm., Senior Regulatory Affairs Manager
Charlotte Lindorf Eriksen
Cand.med.vet./DVM, Head of Pharmacovigilance & QPPV - Veterinary accounts
Trine Fabricius Holm
M.Sc.Pharm., Senior Regulatory Affairs Manager
Anne Ravnholdt Høcker
M.Sc. Pharm., Senior Regulatory Affairs Manager
Sana Iqbal
M.Sc.Pharm., Pharmacovigilance Manager & Regulatory Affairs Officer
Lisbeth Bonde Jensen
M.Sc.Pharm., Senior Pharmacovigilance Manager
Jeanette Buskbjerg Poulsen
M.Sc.Pharm., Pharmacovigilance Manager & Deputy QPPV - Human accounts
Karen Jensen
M.Sc.Pharm., Head of Regulatory Affairs
Bettina Jespersen
M.Sc. Pharm., Regulatory Affairs Manager
Bo Kreilgaard
Ph.D.Pharm., Senior Regulatory Affairs Manager
Trine Lorentzen
M.Sc.Pharm., Quality Assurance Manager
Pia Mentz
M.Sc. Pharm., Regulatory Affairs & Pharmacovigilance Manager
Mette Olsen
M.Sc. Pharm., Regulatory Affairs Manager
Katrine Schuster Ovesen
B.Sc.Pharm. and Diploma Engineer, Regulatory Affairs Manager
Mette Skaarup Pedersen
Cand.Scient.Pharm., Regulatory Affairs Manager
Laura Sparving
Cand.Scient.Pharm., Pharmacovigilance Manager & QPPV - Human accounts
Susanne Thiilborg
Ph.D.Pharm., Senior Regulatory Affairs Manager
Services
Registration
We are well-equipped to provide regulatory advice, discuss strategy and/or compile the registration dossier.
Pharmacovigilance
We have a team of highly qualified pharmacovigilance employees with expertise in all aspects of pharmacovigilance.
Translations
We offer high quality medical & pharmaceutical translations into and from several European languages.
Electronic submission
We are equipped to assist with any type of electronic submission and maintenance of your electronic file.
Special medicines areas
Herbal medicinal products, strong vitamin and mineral products, medicinal gasses, euphoriant substances, etc.
GDP & GMP Services
We offer full time and part time responsible person (RP) function and qualified person (QP) function.
Latest News
Are you lacking the capacity or qualification to perform an audit?
At Billev Pharma we have a team of qualified lead auditors within GVP, VGVP, GMP and GDP. Last year our audit team conducted more than 10 remote pharmacovigilance audits and 10 onsite GDP audits of warehouses. We conduct remote and onsite audits within the EU as well...
Simple solutions in a complex PV environment
We are happily handling an increasing number of pharmacovigilance responsibilities for our clients in a complex pharmacovigilance environment. Our team of pharmacovigilance experts is now organised in three different fields – Human Accounts, Veterinary Accounts, and...
Dyrlæger i life science
I det nyeste nummer af Pharma kan du læse om vores kollega Charlotte Lindorf Eriksen og hendes arbejde med pharmacovigilance som dyrlæge i Billev Pharma Pharma nr. 3 2023—Side 14 (ipaper.io). Charlotte er netop blevet forfremmet til Head of Pharmacovigilance og har...