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 1WAVELENGTH ENTERPRISES LTD. Petah Tikva IL
03 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
04 1SRIKEM LABORATORIES PVT. LTD. New Mumbai IN
05 1TAGROS CHEMICALS INDIA PRIVATE LIMITED Chennai IN
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
Certificate Number : R1-CEP 2016-335 - Rev 01
Status : Valid
Issue Date : 2023-05-15
Type : Chemical
Substance Number : 1762
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
Certificate Number : CEP 2017-117 - Rev 05
Status : Valid
Issue Date : 2024-12-13
Type : Chemical
Substance Number : 1762
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Certificate Number : R0-CEP 2021-070 - Rev 00
Status : Valid
Issue Date : 2022-10-04
Type : Chemical
Substance Number : 1762
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PharmaCompass offers a list of Permethrin 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 Permethrin manufacturer or Permethrin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Permethrin manufacturer or Permethrin supplier.
PharmaCompass also assists you with knowing the Permethrin API Price utilized in the formulation of products. Permethrin API Price is not always fixed or binding as the Permethrin Price is obtained through a variety of data sources. The Permethrin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A NIX manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NIX, including repackagers and relabelers. The FDA regulates NIX manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NIX 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 NIX manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A NIX supplier is an individual or a company that provides NIX active pharmaceutical ingredient (API) or NIX finished formulations upon request. The NIX suppliers may include NIX API manufacturers, exporters, distributors and traders.
click here to find a list of NIX suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A NIX CEP of the European Pharmacopoeia monograph is often referred to as a NIX Certificate of Suitability (COS). The purpose of a NIX CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of NIX EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of NIX to their clients by showing that a NIX CEP has been issued for it. The manufacturer submits a NIX CEP (COS) as part of the market authorization procedure, and it takes on the role of a NIX CEP holder for the record. Additionally, the data presented in the NIX CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the NIX DMF.
A NIX CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. NIX 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 NIX suppliers with CEP (COS) on PharmaCompass.
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