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1535868

USP

Cryopreserved Human Fibroblast-Derived Dermal Substitute Reference Photomicrographs (CD)

United States Pharmacopeia (USP)

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About This Item

NACRES:
NA.24
UNSPSC Code:
41116107
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grade

pharmaceutical primary standard

agency

USP

manufacturer/tradename

USP

application(s)

USP Biologics
pharmaceutical
pharmaceutical (small molecule)
pharmaceutical

format

neat

General description

Find answers to frequently asked questions on USP products in USP FAQs.

Cryopreserved Human Fibroblast-Derived Dermal Substitute Reference Photomicrographs serve as visual benchmarks for cryopreserved fibroblast-derived dermal substitutes. These reference standards help in the evaluation of dermal substitutes, ensuring that they maintain their structural integrity and therapeutic efficacy after cryopreservation, crucial for applications in tissue regeneration and skin replacement therapies.

The United States Pharmacopeia (USP) provides quality standards for biologics to ensure their safety, efficacy, and quality throughout the manufacturing process. These standards assist manufacturers in adhering to regulatory requirements and help safeguard public health by reducing risks associated with biologics.

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including MSDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.
For further information and support please go to the website of the issuing Pharmacopoeia.

Analysis Note

These products are for test and assay use only. They are not meant for administration to humans or animals and cannot be used to diagnose, treat, or cure diseases of any kind.  ​

Other Notes

Sales restrictions may apply.
This product is part of the USP Biologics program.
This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including MSDS and any product information leaflets have been developed and issued under the Authority of the issuing Ph
This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including MSDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia. For further information and support please go to the website of the issuing Pharmacopoeia.




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