A new Look for a Growing Organisation

May 22, 2016

We are launching our new website presenting our specialized and dedicated staff and our services within Regulatory Affairs and Pharmacovigilance.

The Billev Pharma team has expanded within the last year. Today, we are 14 around the table. Last week we were 13. Although some say that 13 is an unlucky number, we experience increasing demands for our services, especially within Pharmacovigilance, translations of product information, compilation and submission of MRPs and DCPs for human and veterinary products and compilation of electronic submissions (eCTD, NeeS and VNeeS).

Billev Pharma – Simple Solutions in a Complex Environment

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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.