IOL Chemicals is an innovation-driven bulk drug, Intermediate and Specialty Chemicals company.
01 2IOL CHEMICALS AND PHARMACEUTICALS LTD Ludhiana IN
02 1ARCH PHARMALABS LIMITED Mumbai IN
03 1BASF SE Ludwigshafen DE
04 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
05 1Doctors Organic Chemicals Ltd Tanuku (Po) IN
06 1HUBEI BIOCAUSE HEILEN PHARMACEUTICAL CO., LTD. Jingmen City CN
07 1PIRAMAL PHARMA LIMITED Digwal Village IN
08 1SHANDONG XINHUA PHARMACEUTICAL CO., LTD. Zibo CN
09 1SI GROUP, INC. The Woodlands US
10 2SMS PHARMACEUTICALS LIMITED Hyderabad IN
11 1SOLARA ACTIVE PHARMA SCIENCES LIMITED Chennai IN
12 1ZHEJIANG NHU COMPANY LTD. Shaoxing City CN
IOL Chemicals is an innovation-driven bulk drug, Intermediate and Specialty Chemicals company.
Certificate Number : R0-CEP 2021-506 - Rev 01
Status : Valid
Issue Date : 2023-01-26
Type : Chemical
Substance Number : 721
IOL Chemicals is an innovation-driven bulk drug, Intermediate and Specialty Chemicals company.
Certificate Number : R1-CEP 2008-316 - Rev 05
Status : Valid
Issue Date : 2022-07-27
Type : Chemical
Substance Number : 721
A Gofen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gofen, including repackagers and relabelers. The FDA regulates Gofen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gofen 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 Gofen manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Gofen supplier is an individual or a company that provides Gofen active pharmaceutical ingredient (API) or Gofen finished formulations upon request. The Gofen suppliers may include Gofen API manufacturers, exporters, distributors and traders.
click here to find a list of Gofen suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Gofen CEP of the European Pharmacopoeia monograph is often referred to as a Gofen Certificate of Suitability (COS). The purpose of a Gofen CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Gofen EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Gofen to their clients by showing that a Gofen CEP has been issued for it. The manufacturer submits a Gofen CEP (COS) as part of the market authorization procedure, and it takes on the role of a Gofen CEP holder for the record. Additionally, the data presented in the Gofen CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Gofen DMF.
A Gofen CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Gofen 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 Gofen suppliers with CEP (COS) on PharmaCompass.
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