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 PRIVATE LIMITED 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 02
Status : Valid
Issue Date : 2025-04-16
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 03
Status : Valid
Issue Date : 2025-03-19
Type : Chemical
Substance Number : 727
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A LIDOCAINE AND PRILOCAINE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LIDOCAINE AND PRILOCAINE, including repackagers and relabelers. The FDA regulates LIDOCAINE AND PRILOCAINE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LIDOCAINE AND PRILOCAINE 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 LIDOCAINE AND PRILOCAINE supplier is an individual or a company that provides LIDOCAINE AND PRILOCAINE active pharmaceutical ingredient (API) or LIDOCAINE AND PRILOCAINE finished formulations upon request. The LIDOCAINE AND PRILOCAINE suppliers may include LIDOCAINE AND PRILOCAINE API manufacturers, exporters, distributors and traders.
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A LIDOCAINE AND PRILOCAINE CEP of the European Pharmacopoeia monograph is often referred to as a LIDOCAINE AND PRILOCAINE Certificate of Suitability (COS). The purpose of a LIDOCAINE AND PRILOCAINE CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of LIDOCAINE AND PRILOCAINE EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of LIDOCAINE AND PRILOCAINE to their clients by showing that a LIDOCAINE AND PRILOCAINE CEP has been issued for it. The manufacturer submits a LIDOCAINE AND PRILOCAINE CEP (COS) as part of the market authorization procedure, and it takes on the role of a LIDOCAINE AND PRILOCAINE CEP holder for the record. Additionally, the data presented in the LIDOCAINE AND PRILOCAINE CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the LIDOCAINE AND PRILOCAINE DMF.
A LIDOCAINE AND PRILOCAINE CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. LIDOCAINE AND PRILOCAINE 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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