Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.

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01 1BIOPHORE INDIA PHARMACEUTICALS PVT. LTD. Hyderabad IN
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01 1Nilutamide
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01 1India
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01 1Valid
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 : CEP 2017-225 - Rev 01
Status : Valid
Issue Date : 2024-02-28
Type : Chemical
Substance Number : 2256
55
PharmaCompass offers a list of Nilutamide API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Nilutamide manufacturer or Nilutamide supplier for your needs.
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A Anandron manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Anandron, including repackagers and relabelers. The FDA regulates Anandron manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Anandron 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 Anandron manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Anandron supplier is an individual or a company that provides Anandron active pharmaceutical ingredient (API) or Anandron finished formulations upon request. The Anandron suppliers may include Anandron API manufacturers, exporters, distributors and traders.
click here to find a list of Anandron suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Anandron CEP of the European Pharmacopoeia monograph is often referred to as a Anandron Certificate of Suitability (COS). The purpose of a Anandron CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Anandron EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Anandron to their clients by showing that a Anandron CEP has been issued for it. The manufacturer submits a Anandron CEP (COS) as part of the market authorization procedure, and it takes on the role of a Anandron CEP holder for the record. Additionally, the data presented in the Anandron CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Anandron DMF.
A Anandron CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Anandron 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 Anandron suppliers with CEP (COS) on PharmaCompass.
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