EUROLAB laboratory provides testing and compliance services within the scope of USP 32 NF 27 standard. The specification consists of a set of universal (identification, impurities, assay) and specific tests, one or more analytical procedures for each test, and acceptance criteria. Components are defined as drug substances or excipients.
An excipient is any ingredient other than active ingredients that are intentionally added to the formulation of a dosage form. Excipients are not necessarily inert.
Pharmaceutical substances and excipients may be synthetic, semi-synthetic, derived from nature (natural source) or produced using recombinant technology. Larger molecules and mixtures that require strength testing are often referred to as biological or biotechnological products.
EUROLAB assists manufacturers with USP 32 NF 27 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.
