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Good Manufacturing Practice is a must for the pharmaceutical companies as manufacturers of medicinal products and is a system of internationally recognized rules comprising all aspects of production - staff, premises, equipment, materials, documentation, quality control and aims to provide safety, efficiency and compliance with the pharmacopoeial specification of the medicinal product
These rules are intended for all aspects of the manufacturing process and guarantee the three main regulatory criteria required for the manufacture and use of medicinal products for ensuring efficient treatment - quality, effectiveness and safety.
• Unipharm is the first Bulgarian pharmaceutical manufacturer who has acquired certification for Good Manufacturing Practice by the Bulgarian Drug Agency (BDA) in 1999.
Quality management takes place at two levels:
• Quality Control Department – from input of the medicinal raw materials to output of the finished product.
• Quality Assurance Department in compliance with Good Manufacturing Practice.
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