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01 1MEDILUX LABORATORIES PRIVATE LIMITED Pithampur IN
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01 1Metacresol
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01 1India
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01 1Valid
Certificate Number : CEP 2023-353 - Rev 00
Status : Valid
Issue Date : 2025-03-05
Type : Chemical
Substance Number : 2077
72
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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred M-Cresol manufacturer or M-Cresol supplier.
PharmaCompass also assists you with knowing the M-Cresol API Price utilized in the formulation of products. M-Cresol API Price is not always fixed or binding as the M-Cresol Price is obtained through a variety of data sources. The M-Cresol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CRS manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CRS, including repackagers and relabelers. The FDA regulates CRS manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CRS 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 CRS manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CRS supplier is an individual or a company that provides CRS active pharmaceutical ingredient (API) or CRS finished formulations upon request. The CRS suppliers may include CRS API manufacturers, exporters, distributors and traders.
click here to find a list of CRS suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A CRS CEP of the European Pharmacopoeia monograph is often referred to as a CRS Certificate of Suitability (COS). The purpose of a CRS CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of CRS EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of CRS to their clients by showing that a CRS CEP has been issued for it. The manufacturer submits a CRS CEP (COS) as part of the market authorization procedure, and it takes on the role of a CRS CEP holder for the record. Additionally, the data presented in the CRS CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the CRS DMF.
A CRS CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. CRS 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 CRS suppliers with CEP (COS) on PharmaCompass.
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