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01 Spera Nexus Co., Ltd. (1)
02 Yamamoto Chemical Industry Co., Ltd. (1)
01 Salicylamide (1)
02 Salicylamide "Iwaki" (1)
01 Japan (2)
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PharmaCompass offers a list of Salicylamide 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 Salicylamide manufacturer or Salicylamide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Salicylamide manufacturer or Salicylamide supplier.
PharmaCompass also assists you with knowing the Salicylamide API Price utilized in the formulation of products. Salicylamide API Price is not always fixed or binding as the Salicylamide Price is obtained through a variety of data sources. The Salicylamide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Salicylamide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Salicylamide, including repackagers and relabelers. The FDA regulates Salicylamide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Salicylamide 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 Salicylamide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Salicylamide supplier is an individual or a company that provides Salicylamide active pharmaceutical ingredient (API) or Salicylamide finished formulations upon request. The Salicylamide suppliers may include Salicylamide API manufacturers, exporters, distributors and traders.
click here to find a list of Salicylamide 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 Salicylamide Drug Master File in Japan (Salicylamide JDMF) empowers Salicylamide 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 Salicylamide JDMF during the approval evaluation for pharmaceutical products. At the time of Salicylamide 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 Salicylamide suppliers with JDMF on PharmaCompass.
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