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