Pia Mentz is M.Sc. in Pharmacy and has been with Billev Pharma since July 2021 as a Regulatory Affairs Manager.
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