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.
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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 Urisec 22% Crm manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Urisec 22% Crm, including repackagers and relabelers. The FDA regulates Urisec 22% Crm manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Urisec 22% Crm API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Urisec 22% Crm supplier is an individual or a company that provides Urisec 22% Crm active pharmaceutical ingredient (API) or Urisec 22% Crm finished formulations upon request. The Urisec 22% Crm suppliers may include Urisec 22% Crm API manufacturers, exporters, distributors and traders.
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A Urisec 22% Crm CEP of the European Pharmacopoeia monograph is often referred to as a Urisec 22% Crm Certificate of Suitability (COS). The purpose of a Urisec 22% Crm CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Urisec 22% Crm EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Urisec 22% Crm to their clients by showing that a Urisec 22% Crm CEP has been issued for it. The manufacturer submits a Urisec 22% Crm CEP (COS) as part of the market authorization procedure, and it takes on the role of a Urisec 22% Crm CEP holder for the record. Additionally, the data presented in the Urisec 22% Crm CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Urisec 22% Crm DMF.
A Urisec 22% Crm CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Urisec 22% Crm CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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