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
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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 Mannidex 16700 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mannidex 16700, including repackagers and relabelers. The FDA regulates Mannidex 16700 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mannidex 16700 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 Mannidex 16700 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Mannidex 16700 supplier is an individual or a company that provides Mannidex 16700 active pharmaceutical ingredient (API) or Mannidex 16700 finished formulations upon request. The Mannidex 16700 suppliers may include Mannidex 16700 API manufacturers, exporters, distributors and traders.
click here to find a list of Mannidex 16700 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 Mannidex 16700 Drug Master File in Japan (Mannidex 16700 JDMF) empowers Mannidex 16700 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 Mannidex 16700 JDMF during the approval evaluation for pharmaceutical products. At the time of Mannidex 16700 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 Mannidex 16700 suppliers with JDMF on PharmaCompass.
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