01 1Sakai Chemical Industry Co., Ltd.
01 1Japanese Pharmacopoeia barium sulfate (production only)
01 1Japan
Japanese Pharmacopoeia Barium Sulfate (for manufacturing purposes only)
Registration Number : 217MF10466
Registrant's Address : 5-2 Ebisujimacho, Sakai-ku, Sakai City, Osaka Prefecture
Initial Date of Registration : 2005-08-24
Latest Date of Registration : 2007-07-02
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PharmaCompass offers a list of Barium Sulfate 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 Barium Sulfate manufacturer or Barium Sulfate supplier for your needs.
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PharmaCompass also assists you with knowing the Barium Sulfate API Price utilized in the formulation of products. Barium Sulfate API Price is not always fixed or binding as the Barium Sulfate Price is obtained through a variety of data sources. The Barium Sulfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Liquid Polibar Plus manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Liquid Polibar Plus, including repackagers and relabelers. The FDA regulates Liquid Polibar Plus manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Liquid Polibar Plus 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 Liquid Polibar Plus supplier is an individual or a company that provides Liquid Polibar Plus active pharmaceutical ingredient (API) or Liquid Polibar Plus finished formulations upon request. The Liquid Polibar Plus suppliers may include Liquid Polibar Plus API manufacturers, exporters, distributors and traders.
click here to find a list of Liquid Polibar Plus 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 Liquid Polibar Plus Drug Master File in Japan (Liquid Polibar Plus JDMF) empowers Liquid Polibar Plus 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 Liquid Polibar Plus JDMF during the approval evaluation for pharmaceutical products. At the time of Liquid Polibar Plus 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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