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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A ARESTOCAINE HYDROCHLORIDE W/ LEVONORDEFRIN-1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ARESTOCAINE HYDROCHLORIDE W/ LEVONORDEFRIN-1, including repackagers and relabelers. The FDA regulates ARESTOCAINE HYDROCHLORIDE W/ LEVONORDEFRIN-1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ARESTOCAINE HYDROCHLORIDE W/ LEVONORDEFRIN-1 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 ARESTOCAINE HYDROCHLORIDE W/ LEVONORDEFRIN-1 supplier is an individual or a company that provides ARESTOCAINE HYDROCHLORIDE W/ LEVONORDEFRIN-1 active pharmaceutical ingredient (API) or ARESTOCAINE HYDROCHLORIDE W/ LEVONORDEFRIN-1 finished formulations upon request. The ARESTOCAINE HYDROCHLORIDE W/ LEVONORDEFRIN-1 suppliers may include ARESTOCAINE HYDROCHLORIDE W/ LEVONORDEFRIN-1 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 ARESTOCAINE HYDROCHLORIDE W/ LEVONORDEFRIN-1 Drug Master File in Japan (ARESTOCAINE HYDROCHLORIDE W/ LEVONORDEFRIN-1 JDMF) empowers ARESTOCAINE HYDROCHLORIDE W/ LEVONORDEFRIN-1 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 ARESTOCAINE HYDROCHLORIDE W/ LEVONORDEFRIN-1 JDMF during the approval evaluation for pharmaceutical products. At the time of ARESTOCAINE HYDROCHLORIDE W/ LEVONORDEFRIN-1 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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