01 1Alps Pharmaceutical Co., Ltd.
01 1Methylsulfate N- methyl scopolamine
01 1Japan
N-Methylscopolamine methylsulfate
Registration Number : 217MF11029
Registrant's Address : 2-10-50 Mukaimachi, Furukawa-cho, Hida-shi, Gifu Prefecture
Initial Date of Registration : 2005-12-02
Latest Date of Registration : 2009-10-19
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PharmaCompass offers a list of Methscopolamine Bromide 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 Methscopolamine Bromide manufacturer or Methscopolamine Bromide supplier for your needs.
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A Scopolamine methyl bromide, Pamine, Methscopolamine bromide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Scopolamine methyl bromide, Pamine, Methscopolamine bromide, including repackagers and relabelers. The FDA regulates Scopolamine methyl bromide, Pamine, Methscopolamine bromide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Scopolamine methyl bromide, Pamine, Methscopolamine bromide 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 Scopolamine methyl bromide, Pamine, Methscopolamine bromide supplier is an individual or a company that provides Scopolamine methyl bromide, Pamine, Methscopolamine bromide active pharmaceutical ingredient (API) or Scopolamine methyl bromide, Pamine, Methscopolamine bromide finished formulations upon request. The Scopolamine methyl bromide, Pamine, Methscopolamine bromide suppliers may include Scopolamine methyl bromide, Pamine, Methscopolamine bromide 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 Scopolamine methyl bromide, Pamine, Methscopolamine bromide Drug Master File in Japan (Scopolamine methyl bromide, Pamine, Methscopolamine bromide JDMF) empowers Scopolamine methyl bromide, Pamine, Methscopolamine bromide 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 Scopolamine methyl bromide, Pamine, Methscopolamine bromide JDMF during the approval evaluation for pharmaceutical products. At the time of Scopolamine methyl bromide, Pamine, Methscopolamine bromide 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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