EUROLAB laboratory provides testing and compliance services within the scope of 21 CFR Part 210 standard. It outlines the minimum GMP requirements covering production, facilities and controls for the manufacture, processing, packaging and holding of all medicines to meet safety, quality and purity guidelines.
Compliance with the 21 CFR directive for pharmaceuticals requires effective management of different GMP functions to ensure drug products meet safety, quality, potency and purity requirements.
Automating quality and production management is the most effective way for pharmaceutical companies to collaboratively manage all aspects of pharmaceutical product development.
EUROLAB assists manufacturers with 21 CFR Part 210 test compliance. Our test experts, with their professional working mission and principles, provide you, our manufacturers and suppliers, the best service and controlled testing process in our laboratories. Thanks to these services, businesses receive more effective, high-performance and quality testing services and provide safe, fast and uninterrupted service to their customers.
To get an appointment, to get more detailed information or to request an evaluation, you can ask us to fill in our form and reach you.
EUROLABreporting and certification activities, United Accreditation Foundation (UAF), Turkish Accreditation Agency (TÜRKAK) ve Enterprise Accreditation Foundation (EAF) based on the accreditation provided by the accreditation body. The Enterprise Accreditation Foundation (EAF) accreditation body is also a signatory of the United Nations (UN GLOBAL COMPACT) organization.
