01 1BIOINDUSTRIA L.I.M. S.P.A. Novi Ligure IT
01 1Prazosin hydrochloride
01 1Italy
01 1Valid
Certificate Number : R1-CEP 2004-221 - Rev 03
Status : Valid
Issue Date : 2021-06-07
Type : Chemical
Substance Number : 856
45
PharmaCompass offers a list of Prazosin Hydrochloride 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 Prazosin Hydrochloride manufacturer or Prazosin Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Prazosin Hydrochloride API Price utilized in the formulation of products. Prazosin Hydrochloride API Price is not always fixed or binding as the Prazosin Hydrochloride Price is obtained through a variety of data sources. The Prazosin Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AF-0012 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AF-0012, including repackagers and relabelers. The FDA regulates AF-0012 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AF-0012 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 AF-0012 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A AF-0012 supplier is an individual or a company that provides AF-0012 active pharmaceutical ingredient (API) or AF-0012 finished formulations upon request. The AF-0012 suppliers may include AF-0012 API manufacturers, exporters, distributors and traders.
click here to find a list of AF-0012 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A AF-0012 CEP of the European Pharmacopoeia monograph is often referred to as a AF-0012 Certificate of Suitability (COS). The purpose of a AF-0012 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of AF-0012 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of AF-0012 to their clients by showing that a AF-0012 CEP has been issued for it. The manufacturer submits a AF-0012 CEP (COS) as part of the market authorization procedure, and it takes on the role of a AF-0012 CEP holder for the record. Additionally, the data presented in the AF-0012 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the AF-0012 DMF.
A AF-0012 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. AF-0012 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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