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