Bioprocessing
Accelerate your biologic
drug development with
Purolite™ chromatography resins.
Accelerate your biologic
drug development with
Purolite™ chromatography resins.
En tant que leader mondial de la technologie des résines, nous développons et fabriquons de petites billes qui sont utilisées dans les industries les plus réglementées au monde pour séparer, éliminer ou récupérer des éléments et composés très spécifiques.
Apprendre encore plusAvec 40 ans d'expertise en fabrication et 30 ans d'expérience en réglementation, nous fournissons des technologies de séparation, de purification et d'extraction de pointe pour soutenir les applications de chromatographie et de biocatalyse dans les soins de santé et les sciences de la vie.
(Pages Sciences de la vie actuellement en anglais uniquement)
Nous sommes le leader mondial des technologies de séparation, de purification et d'extraction à base de résine, qui fournissent des solutions durables pour notre environnement, nos entreprises et nos soins de santé.
Learn MoreNos équipes de support technique et de service toujours prêtes font un pas supplémentaire pour devenir votre ressource la plus fiable. Nous sommes là pour vous.
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 of our Pharma and Medical products are produced in our ISO-certified production facilities in the UK, Romania, China and the USA. Ecolab 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.