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01 1Albert David Ltd Calcutta IN
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01 1Chlorpropamide
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01 1India
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01 1Withdrawn by EDQM Failure to CEP procedure
Certificate Number : R1-CEP 2000-020 - Rev 01
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2008-10-08
Type : Chemical
Substance Number : 1087
71
PharmaCompass offers a list of Chlorpropamide 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 Chlorpropamide manufacturer or Chlorpropamide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Chlorpropamide manufacturer or Chlorpropamide supplier.
PharmaCompass also assists you with knowing the Chlorpropamide API Price utilized in the formulation of products. Chlorpropamide API Price is not always fixed or binding as the Chlorpropamide Price is obtained through a variety of data sources. The Chlorpropamide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A dia benese manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of dia benese, including repackagers and relabelers. The FDA regulates dia benese manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. dia benese 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 dia benese supplier is an individual or a company that provides dia benese active pharmaceutical ingredient (API) or dia benese finished formulations upon request. The dia benese suppliers may include dia benese API manufacturers, exporters, distributors and traders.
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A dia benese CEP of the European Pharmacopoeia monograph is often referred to as a dia benese Certificate of Suitability (COS). The purpose of a dia benese CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of dia benese EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of dia benese to their clients by showing that a dia benese CEP has been issued for it. The manufacturer submits a dia benese CEP (COS) as part of the market authorization procedure, and it takes on the role of a dia benese CEP holder for the record. Additionally, the data presented in the dia benese CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the dia benese DMF.
A dia benese CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. dia benese 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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