01 2Kyowa Chemical Industry Co., Ltd.
01 2Japanese Pharmacopoeia synthetic aluminum silicate (manufacturing only)
01 2Japan
Japanese Pharmacopoeia Synthetic Aluminum Silicate (for manufacturing only)
Registration Number : 221MF10268
Registrant's Address : 305 Yashima Nishimachi, Takamatsu City, Kagawa Prefecture
Initial Date of Registration : 2009-12-07
Latest Date of Registration : 2009-12-07
Japanese Pharmacopoeia Synthetic Aluminum Silicate (for manufacturing only)
Registration Number : 221MF10267
Registrant's Address : 305 Yashima Nishimachi, Takamatsu City, Kagawa Prefecture
Initial Date of Registration : 2009-12-07
Latest Date of Registration : 2009-12-07
A Silicic Acid (H6Si2O7), Aluminum Salt (1:2) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Silicic Acid (H6Si2O7), Aluminum Salt (1:2), including repackagers and relabelers. The FDA regulates Silicic Acid (H6Si2O7), Aluminum Salt (1:2) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Silicic Acid (H6Si2O7), Aluminum Salt (1:2) API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Silicic Acid (H6Si2O7), Aluminum Salt (1:2) supplier is an individual or a company that provides Silicic Acid (H6Si2O7), Aluminum Salt (1:2) active pharmaceutical ingredient (API) or Silicic Acid (H6Si2O7), Aluminum Salt (1:2) finished formulations upon request. The Silicic Acid (H6Si2O7), Aluminum Salt (1:2) suppliers may include Silicic Acid (H6Si2O7), Aluminum Salt (1:2) API manufacturers, exporters, distributors and traders.
click here to find a list of Silicic Acid (H6Si2O7), Aluminum Salt (1:2) 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 Silicic Acid (H6Si2O7), Aluminum Salt (1:2) Drug Master File in Japan (Silicic Acid (H6Si2O7), Aluminum Salt (1:2) JDMF) empowers Silicic Acid (H6Si2O7), Aluminum Salt (1:2) 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 Silicic Acid (H6Si2O7), Aluminum Salt (1:2) JDMF during the approval evaluation for pharmaceutical products. At the time of Silicic Acid (H6Si2O7), Aluminum Salt (1:2) 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 Silicic Acid (H6Si2O7), Aluminum Salt (1:2) suppliers with JDMF on PharmaCompass.
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