01 1CONCORD BIOTECH LIMITED Ahmedabad IN
01 1Mycophenolate mofetil, By azeotropic distillation
01 1India
01 1Valid
Mycophenolate Mofetil, By Azeotropic Distillatio...
Certificate Number : CEP 2018-157 - Rev 02
Status : Valid
Issue Date : 2024-02-09
Type : Chemical
Substance Number : 1700
74
PharmaCompass offers a list of Mycophenolic Acid 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 Mycophenolic Acid manufacturer or Mycophenolic Acid supplier for your needs.
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PharmaCompass also assists you with knowing the Mycophenolic Acid API Price utilized in the formulation of products. Mycophenolic Acid API Price is not always fixed or binding as the Mycophenolic Acid Price is obtained through a variety of data sources. The Mycophenolic Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MOA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MOA, including repackagers and relabelers. The FDA regulates MOA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MOA 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 MOA supplier is an individual or a company that provides MOA active pharmaceutical ingredient (API) or MOA finished formulations upon request. The MOA suppliers may include MOA API manufacturers, exporters, distributors and traders.
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A MOA CEP of the European Pharmacopoeia monograph is often referred to as a MOA Certificate of Suitability (COS). The purpose of a MOA CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of MOA EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of MOA to their clients by showing that a MOA CEP has been issued for it. The manufacturer submits a MOA CEP (COS) as part of the market authorization procedure, and it takes on the role of a MOA CEP holder for the record. Additionally, the data presented in the MOA CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the MOA DMF.
A MOA CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. MOA 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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