01 1Biosensors International
01 1BIOLIMUS A9 A PHARMACEUTICAL INGREDIENT (API)
01 1Singapore
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23285
Submission : 2009-12-24
Status : Inactive
Type : II
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PharmaCompass offers a list of Umirolimus API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Umirolimus manufacturer or Umirolimus supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Umirolimus manufacturer or Umirolimus supplier.
PharmaCompass also assists you with knowing the Umirolimus API Price utilized in the formulation of products. Umirolimus API Price is not always fixed or binding as the Umirolimus Price is obtained through a variety of data sources. The Umirolimus Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Umirolimus manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Umirolimus, including repackagers and relabelers. The FDA regulates Umirolimus manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Umirolimus API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Umirolimus supplier is an individual or a company that provides Umirolimus active pharmaceutical ingredient (API) or Umirolimus finished formulations upon request. The Umirolimus suppliers may include Umirolimus API manufacturers, exporters, distributors and traders.
click here to find a list of Umirolimus suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Umirolimus DMF (Drug Master File) is a document detailing the whole manufacturing process of Umirolimus active pharmaceutical ingredient (API) in detail. Different forms of Umirolimus DMFs exist exist since differing nations have different regulations, such as Umirolimus USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Umirolimus DMF submitted to regulatory agencies in the US is known as a USDMF. Umirolimus USDMF includes data on Umirolimus's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Umirolimus USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Umirolimus suppliers with USDMF on PharmaCompass.
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