Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1MOEHS IBERICA S. L.
02 1Siegfried Evionnaz SA
01 1Hydrochloric acid mepivacaine
02 1MEPIVACAINE HYDROCHLORIDE
01 1Spain
02 1Switzerland
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Registration Number : 228MF10136
Registrant's Address : Cesar Martinell i Brunet 12A, Poligono Rubi Sur, Rubi (Barcelona), Spain
Initial Date of Registration : 2016-07-27
Latest Date of Registration : 2023-08-09
Registration Number : 218MF10524
Registrant's Address : Route du Simplon 1,36,CH-1902 Evionnaz,Switzerland
Initial Date of Registration : 2006-05-18
Latest Date of Registration : 2024-08-28
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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.
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The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Mepivastesin Drug Master File in Japan (Mepivastesin JDMF) empowers Mepivastesin API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Mepivastesin JDMF during the approval evaluation for pharmaceutical products. At the time of Mepivastesin JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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