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
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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, Price,and more, enabling you to easily find the right Fosnetupitant Chloride manufacturer or Fosnetupitant Chloride supplier for your needs.
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PharmaCompass also assists you with knowing the Fosnetupitant Chloride API Price utilized in the formulation of products. Fosnetupitant Chloride API Price is not always fixed or binding as the Fosnetupitant Chloride Price is obtained through a variety of data sources. The Fosnetupitant Chloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Fosnetupitant chloride hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fosnetupitant chloride hydrochloride, including repackagers and relabelers. The FDA regulates Fosnetupitant chloride hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fosnetupitant chloride hydrochloride 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 hydrochloride supplier is an individual or a company that provides Fosnetupitant chloride hydrochloride active pharmaceutical ingredient (API) or Fosnetupitant chloride hydrochloride finished formulations upon request. The Fosnetupitant chloride hydrochloride suppliers may include Fosnetupitant chloride hydrochloride API manufacturers, exporters, distributors and traders.
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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 hydrochloride Drug Master File in Japan (Fosnetupitant chloride hydrochloride JDMF) empowers Fosnetupitant chloride hydrochloride 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 hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Fosnetupitant chloride hydrochloride JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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