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
01 2Diazoxide
01 2India
01 2Valid
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
79
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 DSSTox_CID_2914 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DSSTox_CID_2914, including repackagers and relabelers. The FDA regulates DSSTox_CID_2914 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DSSTox_CID_2914 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 DSSTox_CID_2914 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DSSTox_CID_2914 supplier is an individual or a company that provides DSSTox_CID_2914 active pharmaceutical ingredient (API) or DSSTox_CID_2914 finished formulations upon request. The DSSTox_CID_2914 suppliers may include DSSTox_CID_2914 API manufacturers, exporters, distributors and traders.
click here to find a list of DSSTox_CID_2914 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A DSSTox_CID_2914 CEP of the European Pharmacopoeia monograph is often referred to as a DSSTox_CID_2914 Certificate of Suitability (COS). The purpose of a DSSTox_CID_2914 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of DSSTox_CID_2914 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of DSSTox_CID_2914 to their clients by showing that a DSSTox_CID_2914 CEP has been issued for it. The manufacturer submits a DSSTox_CID_2914 CEP (COS) as part of the market authorization procedure, and it takes on the role of a DSSTox_CID_2914 CEP holder for the record. Additionally, the data presented in the DSSTox_CID_2914 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the DSSTox_CID_2914 DMF.
A DSSTox_CID_2914 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. DSSTox_CID_2914 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 DSSTox_CID_2914 suppliers with CEP (COS) on PharmaCompass.
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