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 global em tecnologia de resina, desenvolvemos e fabricamos pequenos grânulos que são usados nas indústrias mais regulamentadas do mundo para separar, remover ou recuperar elementos e compostos muito específicos.
Saber maisCom 40 anos de experiência em fabricação e 30 anos de experiência regulatória, fornecemos tecnologias líderes de separação, purificação e extração para apoiar aplicações de cromatografia e biocatálise em saúde e ciências da vida.
(Atualmente apenas em inglês)
Somos líderes mundiais em tecnologia de separação, purificação e extração baseada em resina, que fornece soluções sustentáveis para nosso meio ambiente, negócios e saúde.
Learn MoreNosso suporte técnico sempre pronto e equipes de serviço vão além para ser seu recurso mais confiável. Estamos aqui para ajudá-lo.
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.