Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1MOEHS IBERICA S. L.
02 1Daito Co., Ltd.
03 1Dijia Pharmaceutical Group Co. , Ltd.
04 1Ipca Laboratories Limited
05 2Permakem Asia Co., Ltd.
06 1Sanyo Chemical Research Institute Co., Ltd.
07 1Sicor Societa (') Italiana Corticosteroidi S. r. l.
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Registration Number : 219MF10249
Registrant's Address : Cesar Martinell i Brunet 12A, Poligono Rubi Sur, Rubi (Barcelona), Spain
Initial Date of Registration : 2007-07-26
Latest Date of Registration : 2013-05-10
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PharmaCompass offers a list of Nifedipine 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 Nifedipine manufacturer or Nifedipine supplier for your needs.
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A N0528 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of N0528, including repackagers and relabelers. The FDA regulates N0528 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. N0528 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 N0528 supplier is an individual or a company that provides N0528 active pharmaceutical ingredient (API) or N0528 finished formulations upon request. The N0528 suppliers may include N0528 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 N0528 Drug Master File in Japan (N0528 JDMF) empowers N0528 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 N0528 JDMF during the approval evaluation for pharmaceutical products. At the time of N0528 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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