As of January 2020, Susanne Thiilborg and Bo Kreilgaard will hold the position of Senior Regulatory Affairs Manager and Lisbeth Bonde Jensen now holds the position of Senior Pharmacovigilance Manager. Lisbeth is also QPPV for one of our major accounts.
Lisbeth, Susanne and Bo have more than 20 years of experience within their respective field. You can read more about their 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.