01 1Qingdao Taidong Pharmaceutical Co., Ltd.
01 1DL- methionine
01 1China
Registration Number : 219MF10244
Registrant's Address : No. 22, Huahai Road, Chengyang District, Qingdao City (Huanhai Economic Development Z...
Initial Date of Registration : 2007-07-17
Latest Date of Registration : 2007-07-17
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PharmaCompass offers a list of Methionine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Methionine manufacturer or Methionine supplier for your needs.
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A Pedameth manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pedameth, including repackagers and relabelers. The FDA regulates Pedameth manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pedameth API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Pedameth manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Pedameth supplier is an individual or a company that provides Pedameth active pharmaceutical ingredient (API) or Pedameth finished formulations upon request. The Pedameth suppliers may include Pedameth API manufacturers, exporters, distributors and traders.
click here to find a list of Pedameth suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
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 Pedameth Drug Master File in Japan (Pedameth JDMF) empowers Pedameth 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 Pedameth JDMF during the approval evaluation for pharmaceutical products. At the time of Pedameth JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Pedameth suppliers with JDMF on PharmaCompass.
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