01 1FORMOSA LABORATORIES, INC.
01 1Nonyl acid Waniriruamido
01 1Taiwan
Registration Number : 222MF10228
Registrant's Address : 36 Hoping Street, Louchu, Taoyuan 33842, Taiwan
Initial Date of Registration : 2010-09-10
Latest Date of Registration : 2010-09-10
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PharmaCompass offers a list of Nonivamide 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 Nonivamide manufacturer or Nonivamide supplier for your needs.
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PharmaCompass also assists you with knowing the Nonivamide API Price utilized in the formulation of products. Nonivamide API Price is not always fixed or binding as the Nonivamide Price is obtained through a variety of data sources. The Nonivamide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A N-Pelargonic Acid Vanillylamide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of N-Pelargonic Acid Vanillylamide, including repackagers and relabelers. The FDA regulates N-Pelargonic Acid Vanillylamide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. N-Pelargonic Acid Vanillylamide 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 N-Pelargonic Acid Vanillylamide supplier is an individual or a company that provides N-Pelargonic Acid Vanillylamide active pharmaceutical ingredient (API) or N-Pelargonic Acid Vanillylamide finished formulations upon request. The N-Pelargonic Acid Vanillylamide suppliers may include N-Pelargonic Acid Vanillylamide 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 N-Pelargonic Acid Vanillylamide Drug Master File in Japan (N-Pelargonic Acid Vanillylamide JDMF) empowers N-Pelargonic Acid Vanillylamide 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 N-Pelargonic Acid Vanillylamide JDMF during the approval evaluation for pharmaceutical products. At the time of N-Pelargonic Acid Vanillylamide 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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