M.Sc. Pharm., Senior Regulatory Affairs Manager
Mette Olsen is M.Sc. in Pharmacy and has been with Billev Pharma since May 2021 as Senior Regulatory Affairs Manager.
Mette has a Marketing Compliance Academy Diploma from Atrium.
Mette’s experience covers:
- 15+ years of experience within Regulatory Affairs handling procedures within the EU from Global Danish Pharmaceutical Companies.
- 6 years of experience within Pharmacovigilance activities from Global Danish Pharmaceutical Companies.
- 8 years of experience with Marketing Compliance in Nordic Countries.
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 Pharmacovigilance Specialist – Stillingen er besat
Har du erfaring med pharmacovigilance - og søger du spændende arbejdsopgaver og stor 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 avancerede PV-opgaver på...
Vi søger erfaren CMC-specialist – Stillingen er besat
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...
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