Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1Moehs Iberica S.L. Rubi ES
02 1S.I.M.S. S.R.L. Reggello IT
03 1SIEGFRIED EVIONNAZ SA Evionnaz CH
01 3Mepivacaine hydrochloride
01 1Italy
02 1Spain
03 1Switzerland
01 3Valid
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 : R1-CEP 2004-205 - Rev 02
Status : Valid
Issue Date : 2018-11-08
Type : Chemical
Substance Number : 1242
Certificate Number : R1-CEP 2001-305 - Rev 04
Status : Valid
Issue Date : 2018-11-08
Type : Chemical
Substance Number : 1242
Certificate Number : R1-CEP 2010-129 - Rev 02
Status : Valid
Issue Date : 2019-08-01
Type : Chemical
Substance Number : 1242
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PharmaCompass offers a list of Mepivacaine Hydrochloride 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 Mepivacaine Hydrochloride manufacturer or Mepivacaine Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Mepivacaine Hydrochloride API Price utilized in the formulation of products. Mepivacaine Hydrochloride API Price is not always fixed or binding as the Mepivacaine Hydrochloride Price is obtained through a variety of data sources. The Mepivacaine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Mepivastesin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mepivastesin, including repackagers and relabelers. The FDA regulates Mepivastesin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mepivastesin 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 Mepivastesin supplier is an individual or a company that provides Mepivastesin active pharmaceutical ingredient (API) or Mepivastesin finished formulations upon request. The Mepivastesin suppliers may include Mepivastesin API manufacturers, exporters, distributors and traders.
click here to find a list of Mepivastesin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Mepivastesin CEP of the European Pharmacopoeia monograph is often referred to as a Mepivastesin Certificate of Suitability (COS). The purpose of a Mepivastesin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Mepivastesin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Mepivastesin to their clients by showing that a Mepivastesin CEP has been issued for it. The manufacturer submits a Mepivastesin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Mepivastesin CEP holder for the record. Additionally, the data presented in the Mepivastesin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Mepivastesin DMF.
A Mepivastesin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Mepivastesin 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 Mepivastesin suppliers with CEP (COS) on PharmaCompass.
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