Anja van Arkens
M.Sc.Pharm., Director & Owner
Ulrikke Lynge Jensen
M.Sc.Pharm., Director & Owner
Amalie Gjøl Almegaard
B.Sc. Nursing, Master of Arts in Educational Psychology, Pharmacovigilance Officer
Maria Brogaard
Senior State-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 & Deputy QPPV - Major accounts
Rikke Heidmann
Cand.med.vet/DVM, Senior Pharmacovigilance Manager
Jeanette Buskbjerg Poulsen
M.Sc.Pharm., Pharmacovigilance Manager & QPPV - Human accounts
Karen Jensen
M.Sc.Pharm., Head of Regulatory Affairs
Bettina Jespersen
M.Sc. Pharm., Regulatory Affairs Manager
Anne Liborius
Medical Degree/MD, PgD, Senior Pharmacovigilance Manager & Deputy QPPV – Human accounts
Susanne Thiilborg
Ph.D.Pharm., Senior Regulatory Affairs Manager
Mette Skaarup Pedersen
Cand.Scient.Pharm., Senior Regulatory Affairs Manager
Trine Lorentzen
M.Sc.Pharm., Quality Assurance Manager
Pia Mentz
M.Sc. Pharm., Senior Regulatory Affairs & Pharmacovigilance Manager
Mette Olsen
M.Sc. Pharm., Senior Regulatory Affairs Manager
Katrine Schuster Ovesen
B.Sc.Pharm. and Diploma Engineer, 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
Vi søger erfaren CMC-specialist
Er du ekspert i RA CMC og søger du spændende arbejdsopgaver og fleksibilitet i din hverdag? Så er du måske den kollega, vi leder efter! Hos Billev Pharma ApS tilbyder vi en spændende mulighed for at arbejde med avanceret farmaceutisk og analytisk regulatorisk...
En inspirerende teamdag
Hvordan kan det være, at nogle ser begyndelser (bryllup), mens andre ser slutninger (begravelse), når 4 sorte limousiner kommer kørende i kortege på tværs af vejen? Kan du lære at holde hovedet, håbet, humøret & modet oppe? JA, vi nåede 9 opbyggelige øvelser på 5...
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...