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 1EDMOND PHARMA S.R.L. Paderno Dugnano IT
03 1EMCURE PHARMACEUTICALS LIMITED Pune IN
04 1HARMAN FINOCHEM LIMITED Mumbai IN
01 4Isoprenaline hydrochloride
01 3India
02 1Sweden
01 4Valid
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 : R1-CEP 2017-180 - Rev 00
Status : Valid
Issue Date : 2023-07-05
Type : Chemical
Substance Number : 1332
Certificate Number : R0-CEP 2022-154 - Rev 00
Status : Valid
Issue Date : 2023-07-21
Type : Chemical
Substance Number : 1332
Certificate Number : CEP 2019-148 - Rev 01
Status : Valid
Issue Date : 2024-09-30
Type : Chemical
Substance Number : 1332
Certificate Number : CEP 2022-088 - Rev 00
Status : Valid
Issue Date : 2024-05-15
Type : Chemical
Substance Number : 1332
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PharmaCompass offers a list of Isoproterenol 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 Isoproterenol manufacturer or Isoproterenol supplier for your needs.
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PharmaCompass also assists you with knowing the Isoproterenol API Price utilized in the formulation of products. Isoproterenol API Price is not always fixed or binding as the Isoproterenol Price is obtained through a variety of data sources. The Isoproterenol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Aludrine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aludrine, including repackagers and relabelers. The FDA regulates Aludrine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aludrine 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 Aludrine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Aludrine supplier is an individual or a company that provides Aludrine active pharmaceutical ingredient (API) or Aludrine finished formulations upon request. The Aludrine suppliers may include Aludrine API manufacturers, exporters, distributors and traders.
click here to find a list of Aludrine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Aludrine CEP of the European Pharmacopoeia monograph is often referred to as a Aludrine Certificate of Suitability (COS). The purpose of a Aludrine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Aludrine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Aludrine to their clients by showing that a Aludrine CEP has been issued for it. The manufacturer submits a Aludrine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Aludrine CEP holder for the record. Additionally, the data presented in the Aludrine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Aludrine DMF.
A Aludrine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Aludrine 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 Aludrine suppliers with CEP (COS) on PharmaCompass.
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