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, and more, enabling you to easily find the right Nonivamide manufacturer or Nonivamide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nonivamide manufacturer or Nonivamide supplier.
A N-vanillylnonanamide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of N-vanillylnonanamide, including repackagers and relabelers. The FDA regulates N-vanillylnonanamide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. N-vanillylnonanamide 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 N-vanillylnonanamide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A N-vanillylnonanamide supplier is an individual or a company that provides N-vanillylnonanamide active pharmaceutical ingredient (API) or N-vanillylnonanamide finished formulations upon request. The N-vanillylnonanamide suppliers may include N-vanillylnonanamide API manufacturers, exporters, distributors and traders.
click here to find a list of N-vanillylnonanamide suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 N-vanillylnonanamide Drug Master File in Japan (N-vanillylnonanamide JDMF) empowers N-vanillylnonanamide 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-vanillylnonanamide JDMF during the approval evaluation for pharmaceutical products. At the time of N-vanillylnonanamide 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 N-vanillylnonanamide suppliers with JDMF on PharmaCompass.
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