Bioprocessing (English only)
DurA Cycle A50
Driving innovation and performance while
reducing cost of goods.
DurA Cycle A50
Driving innovation and performance while
reducing cost of goods.
私たちは樹脂技術のグローバルリーダーとして、世界で最も規制の厳しい産業で、非常に特殊な元素や化合物を分離、除去、回収するために使用される小型ビーズを開発・製造しています。
もっと読むWith 40 years of manufacturing expertise and 30 years of regulatory experience, we supply leading separation, purification and extraction technologies to support chromatography applications within the Pharma and Medical space.
Learn moreWe are a world leader in resin-based separation, purification and extraction technology, that provides sustainable solutions for our environment, businesses and healthcare.
Learn More私たちの常に準備ができている技術サポートとサービスチームは、あなたの最も信頼できるリソースになるために追加のステップを踏み出します。私たちはあなたのためにここにいます。
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.