01 2BioLife Solutions, Inc. ，
02 1Gaylord Chemical Company, LLC
01 1Dimethyl Sulfoxide
02 1Raw materials for cell processing, etc. ・ CryoStor CS10 Preservation Media Solution
03 1Raw materials for cell processing, etc. ・ CryoStor CS5 Preservation Media Solution
01 3U.S.A
Raw materials for cell processing, etc. CryoStor CS5 Preservation Media Solution
Registration Number : 303MF40046
Registrant's Address : 3303 Monte Villa Parkway Suite 310 Bothell, WA 98021 USA
Initial Date of Registration : 2021-07-28
Latest Date of Registration : 2021-07-28
Raw materials for cell processing, etc. CryoStor CS10 Preservation Media Solution
Registration Number : 302MF40040
Registrant's Address : 3303 Monte Villa Parkway Suite 310 Bothell, WA 98021 USA
Initial Date of Registration : 2020-10-21
Latest Date of Registration : 2020-10-29
Registration Number : 301MF10105
Registrant's Address : 106 Galeria Blvd Slidell, LA 70458, USA
Initial Date of Registration : 2019-12-10
Latest Date of Registration : 2019-12-10
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PharmaCompass offers a list of Dimethyl Sulfoxide 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 Dimethyl Sulfoxide manufacturer or Dimethyl Sulfoxide supplier for your needs.
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PharmaCompass also assists you with knowing the Dimethyl Sulfoxide API Price utilized in the formulation of products. Dimethyl Sulfoxide API Price is not always fixed or binding as the Dimethyl Sulfoxide Price is obtained through a variety of data sources. The Dimethyl Sulfoxide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Diluent manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diluent, including repackagers and relabelers. The FDA regulates Diluent manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diluent 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 Diluent supplier is an individual or a company that provides Diluent active pharmaceutical ingredient (API) or Diluent finished formulations upon request. The Diluent suppliers may include Diluent 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 Diluent Drug Master File in Japan (Diluent JDMF) empowers Diluent 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 Diluent JDMF during the approval evaluation for pharmaceutical products. At the time of Diluent 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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