Since the very beginning, it has been our vision to be early to provide assistance with the growing amount of new legislation through active participation in the preparatory work for rules and regulations through international organisations. 
This allows us to exchange knowledge and access new information, enabling us to offer a broad range of services and an understanding of the “big picture.”
We can cover all your needs related to product development, regulatory affairs, pharmacovigilance, medical writing, toxicology, GxP, and regulatory informatics. We are specialized in human and veterinary medicines, medical devices and IVDs. During the years we developed certain niche services such as  services for radiopharmaceuticals, bioequivalence studies, bootstrapping, toxicological assessment, compliance with ISO 13485, ISO 20916, ISO 14155. 

Through diligent consultancy work, Billev Pharma East has since its beginning in 2007 slowly grown to its present size also due to loyal customers.

We are building our present services to our customers on this foundation. Therefore, we offer you scientific solutions with beneficial impact on your business processes to gain competitive advantages.

Billev Pharma East Ltd.

Katja Pecjak Reven

This department focuses on providing expert medical guidance and support for therapeutic areas and treatment protocols.

Medical Affairs

This department is responsible for monitoring and ensuring the safety of pharmaceutical products throughout their lifecycle.

Pharmacovigilance Department

This department ensures product quality and compliance with regulatory standards.

Billev Pharma East Ltd.

Org chart

Teams

Medical Affairs

Pharmacovigilance Department

Quality Assurance

Offices

Billev Pharma East Ltd.

Org chart

Teams

Medical Affairs

Pharmacovigilance Department

Quality Assurance

Offices

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