We started 2019 by welcoming 3 new employees in our Billev Pharma team

Apr 26, 2019

Trine Lorentzen, M.Sc. Pharm., filled the recently established post as QA Manager. Trine has several years of solid experience with Good Distribution Practice (GDP) and the function as Responsible Person.

Are you facing an inspection? Are you struggling to keep your QMS up to date? Are you lacking the capacity or qualifications to audit you contract takers or suppliers? Would you like to have an external expert opinion during your self-inspection or audit?

Trine can determine the GAPs in your QMS and help you close them.

Trine has hosted many inspections with impressive results. She is an experienced GDP Lead auditor and conducts her host function in a pleasant and constructive tone with a flash of humour.

You can read more about Trine’s qualifications on our website https://billevpharma.dk/the-billev-pharma-team/

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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.