New Product
DurA Cycle A50
Driving innovation and performance while
reducing cost of goods.
DurA Cycle A50
Driving innovation and performance while
reducing cost of goods.
Como líder mundial en tecnología de resinas, desarrollamos y fabricamos pequeñas perlas que se utilizan en las industrias más reguladas del mundo para separar, eliminar o recuperar elementos y compuestos muy específicos.
Aprende másCon 40 años de experiencia en fabricación y 30 años de experiencia en reglamentación, ofrecemos tecnologías líderes en separación, purificación y extracción para respaldar las aplicaciones de cromatografía y biocatálisis en el cuidado de la salud y las ciencias de la vida.
(Actualmente solo en inglés)
Somos el líder mundial en tecnología de separación, purificación y extracción a base de resina, que brinda soluciones sostenibles para nuestro medio ambiente, negocios y atención médica.
Learn MoreNuestros equipos de servicio y soporte técnico siempre listos dan un paso más para convertirse en su recurso más confiable. Estamos aquí por tí.
Chromatography and biocatalysis resins are utilized in many medical devices for treatment and diagnostic applications. These devices assist patients around the world in managing ailments such as liver and kidney failure, cystic fibrosis, metabolic deficiencies, dementia, diabetes, immunodeficiencies and many more.
We have one of the widest selections of highly pure, pharmaceutical-grade resins for applications requiring either biocatalysis or chromatographic purification, separation and extraction.
Some typical end-user applications for these resins include:
Extracorporeal blood purification (EBP) in dialysis/nanodialysis machines
Purification of foodstuffs used in enteral nutrition (e.g. infant formulas)
Enzyme-based glucose sensors.
Medical devices are required to be compliant with ISO 10993-17:2002, which describes methods and limitations for extractable, leachable and toxicological limits for substances which may leach from the medical device. Polymers used as part of medical devices need to demonstrate their safety and compliance as part of the device to the ISO 10993- 17:2002. This is assured by controlling and defining levels of leachables/extractables, which vary depending on dosage and repetition of use.
Regulatory Information
All Purolite Healthcare & Life Sciences products produced in our ISO-certified production facilities in the UK, Romania, China and the USA. Purolite complies with required national and international regulations, as well as many voluntary specialty certifications. These include:
Part II of the EU GMP Guide
US FDA Current Good Manufacturing Practice (CGMP) regulations
US FDA CFR - Code of Federal Regulations including Title 21
GMO/TSE/BSE free
ResAP(2004)3
NSF/ANSI 61/WRAS standards
REACH regulations
ISO 9001:2015 quality system specifications
ISO 14001:2015 Environmental Management System requirements
OHSAS18001:2007
RoHS Directive 2011/65/EU
Halal and Kosher requirements
We also hold Drug Master Files with the US FDA, Japan, Canada and EU.