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
A Acetylcholine (chloride) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Acetylcholine (chloride), including repackagers and relabelers. The FDA regulates Acetylcholine (chloride) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Acetylcholine (chloride) 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 Acetylcholine (chloride) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Acetylcholine (chloride) supplier is an individual or a company that provides Acetylcholine (chloride) active pharmaceutical ingredient (API) or Acetylcholine (chloride) finished formulations upon request. The Acetylcholine (chloride) suppliers may include Acetylcholine (chloride) API manufacturers, exporters, distributors and traders.
click here to find a list of Acetylcholine (chloride) 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 Acetylcholine (chloride) Drug Master File in Japan (Acetylcholine (chloride) JDMF) empowers Acetylcholine (chloride) 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 Acetylcholine (chloride) JDMF during the approval evaluation for pharmaceutical products. At the time of Acetylcholine (chloride) 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 Acetylcholine (chloride) suppliers with JDMF on PharmaCompass.
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