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 more about Mette’s qualifications here: https://billevpharma.dk/the-billev-pharma-team/
We are well-equipped to provide regulatory advice, discuss strategy and/or compile the registration dossier.
We have a team of highly qualified pharmacovigilance employees with expertise in all aspects of pharmacovigilance.
We offer high quality medical & pharmaceutical translations into and from several European languages.
We are equipped to assist with any type of electronic submission and maintenance of your electronic file.
Herbal medicinal products, strong vitamin and mineral products, medicinal gasses, euphoriant substances, etc.
We offer full time and part time responsible person (RP) function and qualified person (QP) function.