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01 4Tateyama Chemical Co., Ltd.
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01 2Outsider regulations thioctic acid amide (manufactured only)
02 2Thioctic acid
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01 4Japan
Registration Number : 222MF10195
Registrant's Address : 1133 Oe, Imizu City, Toyama Prefecture
Initial Date of Registration : 2010-07-13
Latest Date of Registration : 2010-07-13
Extra-official regulations Thioctic acid amide (for manufacturing only)
Registration Number : 227MF10162
Registrant's Address : 1133 Oe, Imizu City, Toyama Prefecture
Initial Date of Registration : 2015-06-18
Latest Date of Registration : 2015-06-18
Registration Number : 217MF10341
Registrant's Address : 1133 Oe, Imizu City, Toyama Prefecture
Initial Date of Registration : 2005-07-21
Latest Date of Registration : 2009-09-28
Extra-official regulations Thioctic acid amide (for manufacturing only)
Registration Number : 217MF10340
Registrant's Address : 1133 Oe, Imizu City, Toyama Prefecture
Initial Date of Registration : 2005-07-21
Latest Date of Registration : 2010-02-16
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PharmaCompass offers a list of Alpha Lipoic Acid 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 Alpha Lipoic Acid manufacturer or Alpha Lipoic Acid supplier for your needs.
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A Alpha Lipon Stada manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Alpha Lipon Stada, including repackagers and relabelers. The FDA regulates Alpha Lipon Stada manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Alpha Lipon Stada 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 Alpha Lipon Stada supplier is an individual or a company that provides Alpha Lipon Stada active pharmaceutical ingredient (API) or Alpha Lipon Stada finished formulations upon request. The Alpha Lipon Stada suppliers may include Alpha Lipon Stada 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 Alpha Lipon Stada Drug Master File in Japan (Alpha Lipon Stada JDMF) empowers Alpha Lipon Stada 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 Alpha Lipon Stada JDMF during the approval evaluation for pharmaceutical products. At the time of Alpha Lipon Stada 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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