EUROLAB laboratory provides testing and compliance service within the scope of USP 788 standard. This standard specifies the requirements for particulate matter testing for injectables.
Parenteral drug infusions for intramuscular, subcutaneous, or intravenous (IV) injection should be free of visible particles that could be harmful when administered into the bloodstream.
To ensure that these products meet or exceed standards, the particles are detected and quantified using light blocking analysis or microscopic examination after being captured on a filter.
The USP 788 Particulate Matter in Injections general section is used to determine the number and size of undissolved particles in ≥ 10 and ≥ 25 µm injection solutions.
EUROLAB assists manufacturers with USP 788 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.
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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.
