Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 1SANOFI WINTHROP INDUSTRIE Gentilly FR
02 1Farmak A.S. Olomouc CZ
03 1CALYX CHEMICALS AND PHARMACEUTICALS LIMITED Mumbai IN
04 1CENTAUR PHARMACEUTICALS PRIVATE LIMITED Mumbai IN
05 1Industriale Chimica S.R.L. Saronno IT
06 1Joint Stock Company "Grindeks" Riga LV
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Certificate Number : CEP 1996-016 - Rev 14
Status : Valid
Issue Date : 2024-05-06
Type : Chemical
Substance Number : 1060
Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
Certificate Number : R1-CEP 2006-029 - Rev 03
Status : Valid
Issue Date : 2022-06-10
Type : Chemical
Substance Number : 1060
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PharmaCompass offers a list of Zopiclone 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 Zopiclone manufacturer or Zopiclone supplier for your needs.
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PharmaCompass also assists you with knowing the Zopiclone API Price utilized in the formulation of products. Zopiclone API Price is not always fixed or binding as the Zopiclone Price is obtained through a variety of data sources. The Zopiclone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Siaten manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Siaten, including repackagers and relabelers. The FDA regulates Siaten manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Siaten 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 Siaten manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Siaten supplier is an individual or a company that provides Siaten active pharmaceutical ingredient (API) or Siaten finished formulations upon request. The Siaten suppliers may include Siaten API manufacturers, exporters, distributors and traders.
click here to find a list of Siaten suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Siaten CEP of the European Pharmacopoeia monograph is often referred to as a Siaten Certificate of Suitability (COS). The purpose of a Siaten CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Siaten EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Siaten to their clients by showing that a Siaten CEP has been issued for it. The manufacturer submits a Siaten CEP (COS) as part of the market authorization procedure, and it takes on the role of a Siaten CEP holder for the record. Additionally, the data presented in the Siaten CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Siaten DMF.
A Siaten CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Siaten 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 Siaten suppliers with CEP (COS) on PharmaCompass.
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