01 1SEKISUI MEDICAL CO., LTD. Tokyo JP
01 1Clemastine fumarate
01 1Japan
01 1Valid
Certificate Number : R1-CEP 2001-262 - Rev 04
Status : Valid
Issue Date : 2017-02-17
Type : Chemical
Substance Number : 1190
38
PharmaCompass offers a list of Clemastine 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 Clemastine manufacturer or Clemastine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Clemastine manufacturer or Clemastine supplier.
PharmaCompass also assists you with knowing the Clemastine API Price utilized in the formulation of products. Clemastine API Price is not always fixed or binding as the Clemastine Price is obtained through a variety of data sources. The Clemastine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Clemastine Fumarate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Clemastine Fumarate, including repackagers and relabelers. The FDA regulates Clemastine Fumarate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Clemastine Fumarate 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 Clemastine Fumarate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Clemastine Fumarate supplier is an individual or a company that provides Clemastine Fumarate active pharmaceutical ingredient (API) or Clemastine Fumarate finished formulations upon request. The Clemastine Fumarate suppliers may include Clemastine Fumarate API manufacturers, exporters, distributors and traders.
click here to find a list of Clemastine Fumarate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Clemastine Fumarate CEP of the European Pharmacopoeia monograph is often referred to as a Clemastine Fumarate Certificate of Suitability (COS). The purpose of a Clemastine Fumarate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Clemastine Fumarate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Clemastine Fumarate to their clients by showing that a Clemastine Fumarate CEP has been issued for it. The manufacturer submits a Clemastine Fumarate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Clemastine Fumarate CEP holder for the record. Additionally, the data presented in the Clemastine Fumarate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Clemastine Fumarate DMF.
A Clemastine Fumarate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Clemastine Fumarate 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 Clemastine Fumarate suppliers with CEP (COS) on PharmaCompass.
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