01 1HAS Healthcare Advanced Synthesis SA
01 1Phosnetupitant chloride hydrochloride
01 1Switzerland
Fosnetupitant chloride hydrochloride
Registration Number : 302MF10154
Registrant's Address : Via Industria, 24 6710 Biasca Switzerland
Initial Date of Registration : 2020-12-15
Latest Date of Registration : 2020-12-15
A Fosnetupitant Chloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fosnetupitant Chloride, including repackagers and relabelers. The FDA regulates Fosnetupitant Chloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fosnetupitant Chloride API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Fosnetupitant Chloride supplier is an individual or a company that provides Fosnetupitant Chloride active pharmaceutical ingredient (API) or Fosnetupitant Chloride finished formulations upon request. The Fosnetupitant Chloride suppliers may include Fosnetupitant Chloride API manufacturers, exporters, distributors and traders.
click here to find a list of Fosnetupitant Chloride 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 Fosnetupitant Chloride Drug Master File in Japan (Fosnetupitant Chloride JDMF) empowers Fosnetupitant Chloride 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 Fosnetupitant Chloride JDMF during the approval evaluation for pharmaceutical products. At the time of Fosnetupitant Chloride 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 Fosnetupitant Chloride suppliers with JDMF on PharmaCompass.
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