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Service description

Biotech manufacturing infrastructure.

Machine park and production capabilities

Capabilities defined on the company profile (read-only)

Full company profile
  • Biyoteknoloji üniteleri
  • GMP üretim hattı
  • İnhalasyon dolum
  • Kalite kontrol laboratuvarı
  • Steril ambalaj

Quality and certifications

Certifications defined on the company profile (read-only)

Full company profile
  • ISO 9001
  • ISO 14001

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Vefa İlaç San. ve Tic. A.Ş.

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The plant is described as equipped with selected latest-generation machines and instruments. Quality control is performed by specialised staff. The Ministry of Health GMP inspection was passed in August 2013; production continues under WHO GMP (pharmaceutical) and ISO 9001:2015. Process and analytical-method validations and new-product stability studies are defined on the R&D and production page as part of the quality system.

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R&D (Galenic and Analytical) — Vefa İlaç San. ve Tic. A.Ş.

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R&D (Galenic and Analytical)

Healthcare & Medical Service

The R&D laboratory has two main units: galenic and analytical. Patent screening, API evaluation, formulation and analytical-method development, process and analytical-method validation, product improvement, new-product stability and CTD dossier preparation are run under QbD (Quality by Design). Vefa İlaç aims to develop innovative products, high-success bioequivalence studies and common CTD files for Turkey and other countries; the R&D lab also runs joint TUBITAK projects.

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Pharmaceutical and Food-Supplement Manufacturing — Vefa İlaç San. ve Tic. A.Ş.

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Pharmaceutical and Food-Supplement Manufacturing

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The Vefa İlaç plant stands on 8,000 m² in total, of which 6,000 m² is indoor. Published annual capacities are 1,425,000,000 solid units (tablets, film-coated tablets, capsules, softgels), 48,000,000 syrups and 15,000,000 creams, ointments and gels. In the soft-gel centre, gelatins run in a closed system and the fill is encapsulated without hand contact. The site holds a WHO GMP (pharmaceutical) certificate.

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