Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1Moehs Iberica S.L. Rubi ES
02 1CAMBREX KARLSKOGA AB Karlskoga SE
03 1DELTA SYNTHETIC CO., LTD. New Taipei City TW
04 1HARMAN FINOCHEM LIMITED Mumbai IN
05 1SOCIETÀ ITALIANA MEDICINALI SCANDICCI S.I.M.S. S.R.L Reggello IT
06 1SWATI SPENTOSE PVT. LTD. Mumbai IN
01 6Lidocaine
01 2India
02 1Italy
03 1Spain
04 1Taiwan
05 1U.S.A
01 6Valid
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Certificate Number : CEP 1998-078 - Rev 06
Status : Valid
Issue Date : 2024-09-23
Type : Chemical
Substance Number : 727
Certificate Number : R1-CEP 2011-326 - Rev 00
Status : Valid
Issue Date : 2018-05-17
Type : Chemical
Substance Number : 727
Certificate Number : R1-CEP 2010-320 - Rev 01
Status : Valid
Issue Date : 2020-07-03
Type : Chemical
Substance Number : 727
Certificate Number : CEP 2014-234 - Rev 01
Status : Valid
Issue Date : 2024-04-03
Type : Chemical
Substance Number : 727
Certificate Number : CEP 2004-156 - Rev 02
Status : Valid
Issue Date : 2024-02-05
Type : Chemical
Substance Number : 727
Certificate Number : CEP 2013-138 - Rev 02
Status : Valid
Issue Date : 2024-09-13
Type : Chemical
Substance Number : 727
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PharmaCompass offers a list of Lidocaine 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 Lidocaine manufacturer or Lidocaine supplier for your needs.
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A LIDODERM manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LIDODERM, including repackagers and relabelers. The FDA regulates LIDODERM manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LIDODERM 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 LIDODERM supplier is an individual or a company that provides LIDODERM active pharmaceutical ingredient (API) or LIDODERM finished formulations upon request. The LIDODERM suppliers may include LIDODERM API manufacturers, exporters, distributors and traders.
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A LIDODERM CEP of the European Pharmacopoeia monograph is often referred to as a LIDODERM Certificate of Suitability (COS). The purpose of a LIDODERM CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of LIDODERM EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of LIDODERM to their clients by showing that a LIDODERM CEP has been issued for it. The manufacturer submits a LIDODERM CEP (COS) as part of the market authorization procedure, and it takes on the role of a LIDODERM CEP holder for the record. Additionally, the data presented in the LIDODERM CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the LIDODERM DMF.
A LIDODERM CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. LIDODERM 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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