01 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
02 1UMICORE ARGENTINA S.A. Pilar Industrial Park AR
01 2Lomustine
01 1Gabon
02 1Germany
01 2Valid
Certificate Number : R0-CEP 2021-132 - Rev 00
Status : Valid
Issue Date : 2022-11-10
Type : Chemical
Substance Number : 928
Certificate Number : CEP 2009-141 - Rev 03
Status : Valid
Issue Date : 2024-08-16
Type : Chemical
Substance Number : 928
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PharmaCompass offers a list of Lomustine 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 Lomustine manufacturer or Lomustine supplier for your needs.
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PharmaCompass also assists you with knowing the Lomustine API Price utilized in the formulation of products. Lomustine API Price is not always fixed or binding as the Lomustine Price is obtained through a variety of data sources. The Lomustine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ICIG 1109 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ICIG 1109, including repackagers and relabelers. The FDA regulates ICIG 1109 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ICIG 1109 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of ICIG 1109 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A ICIG 1109 supplier is an individual or a company that provides ICIG 1109 active pharmaceutical ingredient (API) or ICIG 1109 finished formulations upon request. The ICIG 1109 suppliers may include ICIG 1109 API manufacturers, exporters, distributors and traders.
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A ICIG 1109 CEP of the European Pharmacopoeia monograph is often referred to as a ICIG 1109 Certificate of Suitability (COS). The purpose of a ICIG 1109 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of ICIG 1109 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of ICIG 1109 to their clients by showing that a ICIG 1109 CEP has been issued for it. The manufacturer submits a ICIG 1109 CEP (COS) as part of the market authorization procedure, and it takes on the role of a ICIG 1109 CEP holder for the record. Additionally, the data presented in the ICIG 1109 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the ICIG 1109 DMF.
A ICIG 1109 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. ICIG 1109 CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of ICIG 1109 suppliers with CEP (COS) on PharmaCompass.
