01 1HAS Healthcare Advanced Synthesis SA
01 1HK Innoen Co., Ltd.
01 1Phosnetupitant chloride hydrochloride
01 1Japan
Phosnetupitant chloride hydrochloride
Registrant Name : HK Innoen Co., Ltd.
Registration Date : 2022-10-31
Registration Number : Su203-8-ND
Manufacturer Name : HAS Healthcare Advanced Synt...
Manufacturer Address : Via Industria 24, 6710 Biasca, Switzerland
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PharmaCompass offers a list of Fosnetupitant Chloride 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 Fosnetupitant Chloride manufacturer or Fosnetupitant Chloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fosnetupitant Chloride manufacturer or Fosnetupitant Chloride supplier.
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, and COA related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Fosnetupitant Chloride Drug Master File in Korea (Fosnetupitant Chloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Fosnetupitant Chloride. The MFDS reviews the Fosnetupitant Chloride KDMF as part of the drug registration process and uses the information provided in the Fosnetupitant Chloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Fosnetupitant Chloride KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Fosnetupitant Chloride API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Fosnetupitant Chloride suppliers with KDMF on PharmaCompass.
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