01 1Tokyo Chemical Industry Co., Ltd.
01 1Acetylcholine chloride
01 1Japan
Registration Number : 217MF11159
Registrant's Address : 6-15-9 Toshima, Kita-ku, Tokyo
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2006-10-20
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PharmaCompass also assists you with knowing the Acetylcholine Chloride API Price utilized in the formulation of products. Acetylcholine Chloride API Price is not always fixed or binding as the Acetylcholine Chloride Price is obtained through a variety of data sources. The Acetylcholine Chloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DSSTox_CID_28904 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DSSTox_CID_28904, including repackagers and relabelers. The FDA regulates DSSTox_CID_28904 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DSSTox_CID_28904 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 DSSTox_CID_28904 supplier is an individual or a company that provides DSSTox_CID_28904 active pharmaceutical ingredient (API) or DSSTox_CID_28904 finished formulations upon request. The DSSTox_CID_28904 suppliers may include DSSTox_CID_28904 API manufacturers, exporters, distributors and traders.
click here to find a list of DSSTox_CID_28904 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 DSSTox_CID_28904 Drug Master File in Japan (DSSTox_CID_28904 JDMF) empowers DSSTox_CID_28904 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 DSSTox_CID_28904 JDMF during the approval evaluation for pharmaceutical products. At the time of DSSTox_CID_28904 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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