At Medico Merim, regulatory compliance and product integrity are at the core of our operations. As both a manufacturer and supplier, we ensure that all products we produce or distribute are supported by internationally recognized documentation, meeting the requirements of pharmaceutical authorities, veterinary agencies, and agricultural regulators worldwide.
Our own production lines in Türkiye operate under Good Manufacturing Practices (GMP) and are regularly audited to ensure full compliance with global quality standards. In addition, all partner manufacturers in our network are pre-qualified based on strict regulatory, ethical, and technical criteria.
We proudly provide:
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GMP Certificates – for manufacturing consistency and pharmaceutical-grade quality
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COA (Certificate of Analysis) – detailed batch-specific quality reports
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MSDS (Material Safety Data Sheets) – for chemical safety and handling
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DMF (Drug Master File) Access – for selected APIs and excipients
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Halal & Kosher Compliance – where required by target markets
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Veterinary Production Licenses – for injectable and oral formulations
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Agricultural Product Registrations – aligned with REACH, FAO, and local ministry standards
All documentation is issued by licensed laboratories and is available in English or bilingual formats for ease of registration and importation.
Medico Merim stands for verified quality. Our certificates are not just formalities—they are proof of transparency, trust, and our full commitment to regulatory excellence.