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Turkish Pharmaceutical Firm Set to Meet FMD Compliance Deadline

Adbi Ibrahim is implementing pharmaceutical compliance management and serialization processing software to meet international requirements ahead of the 2019 deadline.

Abdi Ibrahim Esenyurt, Istanbul production complex. (Photo courtesy of Abdi Ibraham.)
Abdi Ibrahim Esenyurt, Istanbul production complex. (Photo courtesy of Abdi Ibraham.)

For Istanbul, Turkey pharmaceutical company Abdi Ibrahim, its business focus centers around the “healing journey.” The company produces antianemic, antibacterial/antiviral, dermatology, endocrine, metabolism, gastrointestinal, cardiovascular, NSAI and myorelaxants, ophthalmology, central nervous system, respiratory and urogenital system products, as well as food supplements, vitamins and minerals from 13 different therapeutic areas.

Founded in 1912, Abdi Ibrahim began as a small pharmacy to the point where today it describes itself as the country’s pharmaceutical industry leader. Abdi Ibrahim operates in 10 countries beyond Turkey. Its portfolio exceeds 180 brands and more than 350 products, which it exports to 50 countries ranging from Canada to the European Union member states, from North Africa to Asia.

With the February 2019 EU Falsified Medicines Directive (FMD) deadline fast approaching, Abdi Ibrahim needed a provider that would enable them to become compliant by the deadline and fulfil its need for new, modern technological operations with data integrity at its core.

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