Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
01 1BIOPHORE INDIA PHARMACEUTICALS PVT. LTD. Hyderabad IN
02 1MSN LABORATORIES PRIVATE LIMITED Rudraram Village IN
03 1Transo-Pharm Produktions-GmbH Siek DE
01 3Diazoxide
01 1Germany
02 2India
01 2Valid
02 1Withdrawn by Holder
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
Certificate Number : R0-CEP 2019-298 - Rev 02
Status : Valid
Issue Date : 2023-05-15
Type : Chemical
Substance Number : 550
Certificate Number : R0-CEP 2021-065 - Rev 00
Status : Valid
Issue Date : 2023-03-03
Type : Chemical
Substance Number : 550
Certificate Number : R1-CEP 2002-140 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2010-04-30
Type : Chemical
Substance Number : 550
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PharmaCompass offers a list of Diazoxide 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 Diazoxide manufacturer or Diazoxide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Diazoxide manufacturer or Diazoxide supplier.
PharmaCompass also assists you with knowing the Diazoxide API Price utilized in the formulation of products. Diazoxide API Price is not always fixed or binding as the Diazoxide Price is obtained through a variety of data sources. The Diazoxide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Hyperstat manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hyperstat, including repackagers and relabelers. The FDA regulates Hyperstat manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hyperstat 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 Hyperstat manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hyperstat supplier is an individual or a company that provides Hyperstat active pharmaceutical ingredient (API) or Hyperstat finished formulations upon request. The Hyperstat suppliers may include Hyperstat API manufacturers, exporters, distributors and traders.
click here to find a list of Hyperstat suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Hyperstat CEP of the European Pharmacopoeia monograph is often referred to as a Hyperstat Certificate of Suitability (COS). The purpose of a Hyperstat CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Hyperstat EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Hyperstat to their clients by showing that a Hyperstat CEP has been issued for it. The manufacturer submits a Hyperstat CEP (COS) as part of the market authorization procedure, and it takes on the role of a Hyperstat CEP holder for the record. Additionally, the data presented in the Hyperstat CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Hyperstat DMF.
A Hyperstat CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Hyperstat 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 Hyperstat suppliers with CEP (COS) on PharmaCompass.
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