Cold and Cryogenic Labeling

Cold and Cryogenic Labeling
Product Description

UPM Raflatac label materials based on the RP Cryo adhesive withstand cryopreservation conditions down to -321 °F (-196 °C), in both vapour phase and liquid nitrogen. The adhesive is extremely resistant to thermal shock, and provides a strong and enduring bond between the label face and PP plastic containers. RP Cryo label materials tolerate multiple freeze-thaw cycles; samples may be thawed in a warm water bath, ice-water or room temperature before returning to cryogenic storage. The labels remain adhered without cracking, peeling, or degrading, ensuring that 100% of the information is secured to identify biological samples for the full duration of their cryogenically extended lifetimes

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UPM Raflatac

  • US
  • 2018
    On CPHI since
  • 1
    Certificates
  • 1000 - 4999
    Employees
Company types
Manufacturer/Innovator
View company profile
Categories
more categories Show less

UPM Raflatac

  • US
  • 2018
    On CPHI since
  • 1
    Certificates
  • 1000 - 4999
    Employees
Company types
Manufacturer/Innovator
View company profile

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UPM Raflatac resources (1)

  • Labeling Solutions Brochure

    Brochure Labeling Solutions Brochure

    This brochure gives an overview of common pharmaceutical and healthcare applications and the UPM Raflatac label solutions that meet these various needs. Every pharmaceutical packaging and labeling solution must comply with strict industry regulations. UPM Raflatac pharmaceutical label materials meet or exceed the following regulatory and safety requirements:EMA (European Medicines Agency)/CVMP/205/04 Guideline on plastic immediate packaging materials 19 May 2005 FDA (Food and Drug Administration, USA) Guidance on Container Closure Systems for Packaging Human Drugs and Biologics (1999) Compliance with 1907/2006/EC (REACH) European food contact regulations; Food Framework Regulation 1935/2004,plastics regulated by EU 10/2011 FDA food contact compliance: FDA 21 CFR 175.105 and 175.125 for adhesives; FDA 21 CFR 176.170 and 176.180 for papersFalsified Medicines Directive (2011/62/EU