EUROLAB laboratory provides testing and compliance service within the scope of USP 661 standard. Officially evaluates plastic products (materials, components and systems) used to package medical products (pharmaceuticals, biologics and dietary supplements).
For plastic packaging to be approved for use with an FDA-approved therapeutic product, data must demonstrate that the material meets USP 661 standards and performance criteria.
Polymers specifically outlined in USP 661 include high-density polyethylene (HDPE), low-density polyethylene (LDPE), polypropylene (PP), polyethylene terephthalate (PET), and polyethylene terephthalate G (PETG), although other polymers are also included in this section. is located. Each material is identified by its properties and unique properties are listed.
The test includes:
EUROLAB assists manufacturers with USP 661 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.
