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, Price,and more, enabling you to easily find the right Methionine manufacturer or Methionine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Methionine manufacturer or Methionine supplier.
PharmaCompass also assists you with knowing the Methionine API Price utilized in the formulation of products. Methionine API Price is not always fixed or binding as the Methionine Price is obtained through a variety of data sources. The Methionine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 0XD manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 0XD, including repackagers and relabelers. The FDA regulates 0XD manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 0XD 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 0XD manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 0XD supplier is an individual or a company that provides 0XD active pharmaceutical ingredient (API) or 0XD finished formulations upon request. The 0XD suppliers may include 0XD API manufacturers, exporters, distributors and traders.
click here to find a list of 0XD suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price 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 0XD Drug Master File in Japan (0XD JDMF) empowers 0XD 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 0XD JDMF during the approval evaluation for pharmaceutical products. At the time of 0XD 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 0XD suppliers with JDMF on PharmaCompass.
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