Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
01 1NOVACYL Ecully FR
02 1API CORPORATION Chuo-ku JP
01 2Methyl salicylate
01 1France
02 1Japan
01 1Valid
02 1Withdrawn by Holder
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
Certificate Number : R2-CEP 1994-007 - Rev 06
Status : Valid
Issue Date : 2019-10-30
Type : Chemical
Substance Number : 230
Certificate Number : R1-CEP 2004-060 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2013-04-09
Type : Chemical
Substance Number : 230
A Methyl Salicylate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Methyl Salicylate, including repackagers and relabelers. The FDA regulates Methyl Salicylate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Methyl Salicylate 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 Methyl Salicylate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Methyl Salicylate supplier is an individual or a company that provides Methyl Salicylate active pharmaceutical ingredient (API) or Methyl Salicylate finished formulations upon request. The Methyl Salicylate suppliers may include Methyl Salicylate API manufacturers, exporters, distributors and traders.
click here to find a list of Methyl Salicylate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Methyl Salicylate CEP of the European Pharmacopoeia monograph is often referred to as a Methyl Salicylate Certificate of Suitability (COS). The purpose of a Methyl Salicylate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Methyl Salicylate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Methyl Salicylate to their clients by showing that a Methyl Salicylate CEP has been issued for it. The manufacturer submits a Methyl Salicylate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Methyl Salicylate CEP holder for the record. Additionally, the data presented in the Methyl Salicylate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Methyl Salicylate DMF.
A Methyl Salicylate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Methyl Salicylate 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 Methyl Salicylate suppliers with CEP (COS) on PharmaCompass.
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