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