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
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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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Prazosin Hydrochloride manufacturer or Prazosin Hydrochloride supplier.
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 Hypovase manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hypovase, including repackagers and relabelers. The FDA regulates Hypovase manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hypovase API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Hypovase supplier is an individual or a company that provides Hypovase active pharmaceutical ingredient (API) or Hypovase finished formulations upon request. The Hypovase suppliers may include Hypovase API manufacturers, exporters, distributors and traders.
click here to find a list of Hypovase suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Hypovase CEP of the European Pharmacopoeia monograph is often referred to as a Hypovase Certificate of Suitability (COS). The purpose of a Hypovase CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Hypovase EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Hypovase to their clients by showing that a Hypovase CEP has been issued for it. The manufacturer submits a Hypovase CEP (COS) as part of the market authorization procedure, and it takes on the role of a Hypovase CEP holder for the record. Additionally, the data presented in the Hypovase CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Hypovase DMF.
A Hypovase CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Hypovase 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 Hypovase suppliers with CEP (COS) on PharmaCompass.
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