Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
01 1BIOPHORE INDIA PHARMACEUTICALS PVT. LTD. Hyderabad IN
01 1Nilutamide
01 1India
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
A Nilandron manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nilandron, including repackagers and relabelers. The FDA regulates Nilandron manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nilandron 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 Nilandron manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nilandron supplier is an individual or a company that provides Nilandron active pharmaceutical ingredient (API) or Nilandron finished formulations upon request. The Nilandron suppliers may include Nilandron API manufacturers, exporters, distributors and traders.
click here to find a list of Nilandron suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Nilandron CEP of the European Pharmacopoeia monograph is often referred to as a Nilandron Certificate of Suitability (COS). The purpose of a Nilandron CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Nilandron EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Nilandron to their clients by showing that a Nilandron CEP has been issued for it. The manufacturer submits a Nilandron CEP (COS) as part of the market authorization procedure, and it takes on the role of a Nilandron CEP holder for the record. Additionally, the data presented in the Nilandron CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Nilandron DMF.
A Nilandron CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Nilandron 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 Nilandron suppliers with CEP (COS) on PharmaCompass.
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