01 1Merck KGaA Darmstadt DE
01 1Urea
01 1Germany
01 1Valid
Certificate Number : R1-CEP 2011-045 - Rev 01
Status : Valid
Issue Date : 2017-11-09
Type : Chemical
Substance Number : 743
51
PharmaCompass offers a list of Urea API 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 Urea API manufacturer or Urea API supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Urea API manufacturer or Urea API supplier.
PharmaCompass also assists you with knowing the Urea API API Price utilized in the formulation of products. Urea API API Price is not always fixed or binding as the Urea API Price is obtained through a variety of data sources. The Urea API Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A URE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of URE, including repackagers and relabelers. The FDA regulates URE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. URE 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 URE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A URE supplier is an individual or a company that provides URE active pharmaceutical ingredient (API) or URE finished formulations upon request. The URE suppliers may include URE API manufacturers, exporters, distributors and traders.
click here to find a list of URE suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A URE CEP of the European Pharmacopoeia monograph is often referred to as a URE Certificate of Suitability (COS). The purpose of a URE CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of URE EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of URE to their clients by showing that a URE CEP has been issued for it. The manufacturer submits a URE CEP (COS) as part of the market authorization procedure, and it takes on the role of a URE CEP holder for the record. Additionally, the data presented in the URE CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the URE DMF.
A URE CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. URE 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 URE suppliers with CEP (COS) on PharmaCompass.
