01 1Jiangsu Hengrui Pharmaceuticals Co., Ltd.
01 1Rihu Healthcare Co., Ltd.
01 1Desflurane
01 1China
Registrant Name : Rihu Healthcare Co., Ltd.
Registration Date : 2023-04-26
Registration Number : 20230426-211-J-1478
Manufacturer Name : Jiangsu Hengrui Pharmaceutic...
Manufacturer Address : 22 Jinqiao Road, Dapu Industrial Park, Economic & Technological Development Zone, Lia...
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PharmaCompass offers a list of Desflurane 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 Desflurane manufacturer or Desflurane supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Desflurane manufacturer or Desflurane supplier.
A Desflurane manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Desflurane, including repackagers and relabelers. The FDA regulates Desflurane manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Desflurane 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 Desflurane manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Desflurane supplier is an individual or a company that provides Desflurane active pharmaceutical ingredient (API) or Desflurane finished formulations upon request. The Desflurane suppliers may include Desflurane API manufacturers, exporters, distributors and traders.
click here to find a list of Desflurane 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 Desflurane Drug Master File in Korea (Desflurane KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Desflurane. The MFDS reviews the Desflurane KDMF as part of the drug registration process and uses the information provided in the Desflurane KDMF to evaluate the safety and efficacy of the drug.
After submitting a Desflurane 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 Desflurane API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Desflurane suppliers with KDMF on PharmaCompass.
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