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
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A Rapidol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rapidol, including repackagers and relabelers. The FDA regulates Rapidol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rapidol API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Rapidol supplier is an individual or a company that provides Rapidol active pharmaceutical ingredient (API) or Rapidol finished formulations upon request. The Rapidol suppliers may include Rapidol API manufacturers, exporters, distributors and traders.
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A Rapidol CEP of the European Pharmacopoeia monograph is often referred to as a Rapidol Certificate of Suitability (COS). The purpose of a Rapidol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Rapidol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Rapidol to their clients by showing that a Rapidol CEP has been issued for it. The manufacturer submits a Rapidol CEP (COS) as part of the market authorization procedure, and it takes on the role of a Rapidol CEP holder for the record. Additionally, the data presented in the Rapidol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Rapidol DMF.
A Rapidol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Rapidol CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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