01 1PCAS Ecully FR
01 1Pindolol
01 1France
01 1Valid
Certificate Number : R1-CEP 1999-195 - Rev 05
Status : Valid
Issue Date : 2022-08-31
Type : Chemical
Substance Number : 634
52
PharmaCompass offers a list of Pindolol 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 Pindolol manufacturer or Pindolol supplier for your needs.
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PharmaCompass also assists you with knowing the Pindolol API Price utilized in the formulation of products. Pindolol API Price is not always fixed or binding as the Pindolol Price is obtained through a variety of data sources. The Pindolol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Visken manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Visken, including repackagers and relabelers. The FDA regulates Visken manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Visken 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 Visken manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Visken supplier is an individual or a company that provides Visken active pharmaceutical ingredient (API) or Visken finished formulations upon request. The Visken suppliers may include Visken API manufacturers, exporters, distributors and traders.
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A Visken CEP of the European Pharmacopoeia monograph is often referred to as a Visken Certificate of Suitability (COS). The purpose of a Visken CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Visken EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Visken to their clients by showing that a Visken CEP has been issued for it. The manufacturer submits a Visken CEP (COS) as part of the market authorization procedure, and it takes on the role of a Visken CEP holder for the record. Additionally, the data presented in the Visken CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Visken DMF.
A Visken CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Visken 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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