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
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PharmaCompass offers a list of Sorbitol 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 Sorbitol API manufacturer or Sorbitol API supplier for your needs.
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PharmaCompass also assists you with knowing the Sorbitol API API Price utilized in the formulation of products. Sorbitol API API Price is not always fixed or binding as the Sorbitol API Price is obtained through a variety of data sources. The Sorbitol API Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Karion instant manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Karion instant, including repackagers and relabelers. The FDA regulates Karion instant manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Karion instant API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Karion instant supplier is an individual or a company that provides Karion instant active pharmaceutical ingredient (API) or Karion instant finished formulations upon request. The Karion instant suppliers may include Karion instant API manufacturers, exporters, distributors and traders.
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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 Karion instant Drug Master File in Japan (Karion instant JDMF) empowers Karion instant 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 Karion instant JDMF during the approval evaluation for pharmaceutical products. At the time of Karion instant JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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