Coral's API range includes Corticosteroids, Antihistamines. Hormones and Antineoplastics.
01 2CORAL DRUGS PRIVATE LIMITED New Delhi IN
02 1AURISCO PHARMACEUTICAL CO., LTD. Tiantai CN
03 1TAPI NL B.V. Amsterdam NL
Coral's API range includes Corticosteroids, Antihistamines. Hormones and Antineoplastics.
Certificate Number : R0-CEP 2022-018 - Rev 00
Status : Valid
Issue Date : 2023-03-06
Type : Chemical
Substance Number : 2768
Coral's API range includes Corticosteroids, Antihistamines. Hormones and Antineoplastics.
Fluticasone Furoate, Process 1
Certificate Number : R0-CEP 2021-372 - Rev 00
Status : Valid
Issue Date : 2023-03-07
Type : Chemical
Substance Number : 2768
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PharmaCompass offers a list of Fluticasone Furoate 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 Fluticasone Furoate manufacturer or Fluticasone Furoate supplier for your needs.
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A BREO ELLIPTA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of BREO ELLIPTA, including repackagers and relabelers. The FDA regulates BREO ELLIPTA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. BREO ELLIPTA 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 BREO ELLIPTA supplier is an individual or a company that provides BREO ELLIPTA active pharmaceutical ingredient (API) or BREO ELLIPTA finished formulations upon request. The BREO ELLIPTA suppliers may include BREO ELLIPTA API manufacturers, exporters, distributors and traders.
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A BREO ELLIPTA CEP of the European Pharmacopoeia monograph is often referred to as a BREO ELLIPTA Certificate of Suitability (COS). The purpose of a BREO ELLIPTA CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of BREO ELLIPTA EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of BREO ELLIPTA to their clients by showing that a BREO ELLIPTA CEP has been issued for it. The manufacturer submits a BREO ELLIPTA CEP (COS) as part of the market authorization procedure, and it takes on the role of a BREO ELLIPTA CEP holder for the record. Additionally, the data presented in the BREO ELLIPTA CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the BREO ELLIPTA DMF.
A BREO ELLIPTA CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. BREO ELLIPTA 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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