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