01 1MEDILUX LABORATORIES PRIVATE LIMITED Pithampur IN
01 1Metacresol
01 1India
01 1Valid
Certificate Number : CEP 2023-353 - Rev 00
Status : Valid
Issue Date : 2025-03-05
Type : Chemical
Substance Number : 2077
35
PharmaCompass offers a list of M-Cresol 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 M-Cresol manufacturer or M-Cresol supplier for your needs.
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A 3-methylcyclohexa-1,3,5-trien-1-ol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 3-methylcyclohexa-1,3,5-trien-1-ol, including repackagers and relabelers. The FDA regulates 3-methylcyclohexa-1,3,5-trien-1-ol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 3-methylcyclohexa-1,3,5-trien-1-ol 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 3-methylcyclohexa-1,3,5-trien-1-ol supplier is an individual or a company that provides 3-methylcyclohexa-1,3,5-trien-1-ol active pharmaceutical ingredient (API) or 3-methylcyclohexa-1,3,5-trien-1-ol finished formulations upon request. The 3-methylcyclohexa-1,3,5-trien-1-ol suppliers may include 3-methylcyclohexa-1,3,5-trien-1-ol API manufacturers, exporters, distributors and traders.
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A 3-methylcyclohexa-1,3,5-trien-1-ol CEP of the European Pharmacopoeia monograph is often referred to as a 3-methylcyclohexa-1,3,5-trien-1-ol Certificate of Suitability (COS). The purpose of a 3-methylcyclohexa-1,3,5-trien-1-ol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 3-methylcyclohexa-1,3,5-trien-1-ol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 3-methylcyclohexa-1,3,5-trien-1-ol to their clients by showing that a 3-methylcyclohexa-1,3,5-trien-1-ol CEP has been issued for it. The manufacturer submits a 3-methylcyclohexa-1,3,5-trien-1-ol CEP (COS) as part of the market authorization procedure, and it takes on the role of a 3-methylcyclohexa-1,3,5-trien-1-ol CEP holder for the record. Additionally, the data presented in the 3-methylcyclohexa-1,3,5-trien-1-ol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 3-methylcyclohexa-1,3,5-trien-1-ol DMF.
A 3-methylcyclohexa-1,3,5-trien-1-ol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 3-methylcyclohexa-1,3,5-trien-1-ol 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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