01 1API CORPORATION Chuo-ku JP
01 1Methyl salicylate
01 1Japan
01 1Withdrawn by Holder
Certificate Number : R1-CEP 2004-060 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2013-04-09
Type : Chemical
Substance Number : 230
49
PharmaCompass offers a list of Methyl Salicylate 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 Methyl Salicylate manufacturer or Methyl Salicylate supplier for your needs.
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PharmaCompass also assists you with knowing the Methyl Salicylate API Price utilized in the formulation of products. Methyl Salicylate API Price is not always fixed or binding as the Methyl Salicylate Price is obtained through a variety of data sources. The Methyl Salicylate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A RTR-003257 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of RTR-003257, including repackagers and relabelers. The FDA regulates RTR-003257 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. RTR-003257 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 RTR-003257 supplier is an individual or a company that provides RTR-003257 active pharmaceutical ingredient (API) or RTR-003257 finished formulations upon request. The RTR-003257 suppliers may include RTR-003257 API manufacturers, exporters, distributors and traders.
click here to find a list of RTR-003257 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A RTR-003257 CEP of the European Pharmacopoeia monograph is often referred to as a RTR-003257 Certificate of Suitability (COS). The purpose of a RTR-003257 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of RTR-003257 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of RTR-003257 to their clients by showing that a RTR-003257 CEP has been issued for it. The manufacturer submits a RTR-003257 CEP (COS) as part of the market authorization procedure, and it takes on the role of a RTR-003257 CEP holder for the record. Additionally, the data presented in the RTR-003257 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the RTR-003257 DMF.
A RTR-003257 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. RTR-003257 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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