01 2Bussan Food Science Co., Ltd.
01 2Japanese Pharmacopoeia D- sorbitol
01 2Japan
Japanese Pharmacopoeia D-Sorbitol
Registration Number : 218MF10315
Registrant's Address : 24-12 Kitahama-cho, Chita City, Aichi Prefecture
Initial Date of Registration : 2006-02-28
Latest Date of Registration : 2006-02-28
Japanese Pharmacopoeia D-Sorbitol
Registration Number : 218MF10314
Registrant's Address : 24-12 Kitahama-cho, Chita City, Aichi Prefecture
Initial Date of Registration : 2006-02-28
Latest Date of Registration : 2006-02-28
A Sorbitol API manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sorbitol API, including repackagers and relabelers. The FDA regulates Sorbitol API manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sorbitol API 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 Sorbitol API manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sorbitol API supplier is an individual or a company that provides Sorbitol API active pharmaceutical ingredient (API) or Sorbitol API finished formulations upon request. The Sorbitol API suppliers may include Sorbitol API API manufacturers, exporters, distributors and traders.
click here to find a list of Sorbitol API 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 Sorbitol API Drug Master File in Japan (Sorbitol API JDMF) empowers Sorbitol API 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 Sorbitol API JDMF during the approval evaluation for pharmaceutical products. At the time of Sorbitol API 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 Sorbitol API suppliers with JDMF on PharmaCompass.
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