01 2Kanto Chemical Co., Ltd.
01 1Potassium hydroxide
02 1Potassium hydroxide (UE-E)
01 2Japan
Registration Number : 219MF10218
Registrant's Address : 3-2-8 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2007-07-06
Latest Date of Registration : 2007-07-06
Registration Number : 219MF10060
Registrant's Address : 3-2-8 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2007-03-05
Latest Date of Registration : 2007-03-05
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PharmaCompass offers a list of Potassium Hydroxide 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 Potassium Hydroxide manufacturer or Potassium Hydroxide supplier for your needs.
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PharmaCompass also assists you with knowing the Potassium Hydroxide API Price utilized in the formulation of products. Potassium Hydroxide API Price is not always fixed or binding as the Potassium Hydroxide Price is obtained through a variety of data sources. The Potassium Hydroxide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 00648_FLUKA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 00648_FLUKA, including repackagers and relabelers. The FDA regulates 00648_FLUKA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 00648_FLUKA 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 00648_FLUKA supplier is an individual or a company that provides 00648_FLUKA active pharmaceutical ingredient (API) or 00648_FLUKA finished formulations upon request. The 00648_FLUKA suppliers may include 00648_FLUKA 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 00648_FLUKA Drug Master File in Japan (00648_FLUKA JDMF) empowers 00648_FLUKA 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 00648_FLUKA JDMF during the approval evaluation for pharmaceutical products. At the time of 00648_FLUKA 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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