01 1EUROAPI HUNGARY Ltd. Budapest HU
02 1PIRAMAL HEALTHCARE UK LIMITED Morpeth GB
01 2Misoprostol
01 1France
02 1U.S.A
01 1Valid
02 1Withdrawn by Holder
Certificate Number : R1-CEP 2010-121 - Rev 01
Status : Valid
Issue Date : 2017-01-20
Type : Chemical
Substance Number : 1731
Certificate Number : R1-CEP 2011-333 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2018-05-17
Type : Chemical
Substance Number : 1731
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PharmaCompass offers a list of Misoprostol 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 Misoprostol manufacturer or Misoprostol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Misoprostol manufacturer or Misoprostol supplier.
PharmaCompass also assists you with knowing the Misoprostol API Price utilized in the formulation of products. Misoprostol API Price is not always fixed or binding as the Misoprostol Price is obtained through a variety of data sources. The Misoprostol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ARTHROTEC-1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ARTHROTEC-1, including repackagers and relabelers. The FDA regulates ARTHROTEC-1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ARTHROTEC-1 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 ARTHROTEC-1 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A ARTHROTEC-1 supplier is an individual or a company that provides ARTHROTEC-1 active pharmaceutical ingredient (API) or ARTHROTEC-1 finished formulations upon request. The ARTHROTEC-1 suppliers may include ARTHROTEC-1 API manufacturers, exporters, distributors and traders.
click here to find a list of ARTHROTEC-1 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A ARTHROTEC-1 CEP of the European Pharmacopoeia monograph is often referred to as a ARTHROTEC-1 Certificate of Suitability (COS). The purpose of a ARTHROTEC-1 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of ARTHROTEC-1 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of ARTHROTEC-1 to their clients by showing that a ARTHROTEC-1 CEP has been issued for it. The manufacturer submits a ARTHROTEC-1 CEP (COS) as part of the market authorization procedure, and it takes on the role of a ARTHROTEC-1 CEP holder for the record. Additionally, the data presented in the ARTHROTEC-1 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the ARTHROTEC-1 DMF.
A ARTHROTEC-1 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. ARTHROTEC-1 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 ARTHROTEC-1 suppliers with CEP (COS) on PharmaCompass.
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