01 1B Food Science Co., Ltd.
01 1Japanese Pharmacopoeia D- mannitol
01 1Japan
Japanese Pharmacopoeia D-Mannitol
Registration Number : 218MF10311
Registrant's Address : 24-12 Kitahamacho, Chita City, Aichi Prefecture
Initial Date of Registration : 2006-02-28
Latest Date of Registration : 2006-02-28
47
PharmaCompass offers a list of Mannitol API 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 Mannitol API manufacturer or Mannitol API supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Mannitol API manufacturer or Mannitol API supplier.
PharmaCompass also assists you with knowing the Mannitol API API Price utilized in the formulation of products. Mannitol API API Price is not always fixed or binding as the Mannitol API Price is obtained through a variety of data sources. The Mannitol API Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Aridol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aridol, including repackagers and relabelers. The FDA regulates Aridol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aridol 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 Aridol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Aridol supplier is an individual or a company that provides Aridol active pharmaceutical ingredient (API) or Aridol finished formulations upon request. The Aridol suppliers may include Aridol API manufacturers, exporters, distributors and traders.
click here to find a list of Aridol 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 Aridol Drug Master File in Japan (Aridol JDMF) empowers Aridol 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 Aridol JDMF during the approval evaluation for pharmaceutical products. At the time of Aridol 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 Aridol suppliers with JDMF on PharmaCompass.
