Pia Mentz
M.Sc. Pharm., Senior Regulatory Affairs & Pharmacovigilance Manager
Pia Mentz is M.Sc. in Pharmacy and has been with Billev Pharma since July 2021 as a Regulatory Affairs Manager. Pia became Regulatory & Pharmacovigilance Manager in January 2023.
Pia has more than 18 years of drug regulatory affairs experience from the Danish Medicines Agency. She has extensive knowledge of the EU human and veterinary pharmaceutical legislation.
Pia´s experience covers:
- Regulatory requirements for human and veterinary medicinal products
- National, MR and DC procedures and other regulatory issues for both human and veterinary medicinal products
- Product information (SmPC, PIL and Labelling) for both human and veterinary medicinal products
- Proofreading of product information and mock-ups
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
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