01 1Central Glass Co., Ltd.
02 1Jiangsu Hengrui Pharmaceuticals Co. , Ltd.
01 1Sevoflurane
02 1Sevoflurane “Hengrui”
01 1China
02 1United Kingdom
Registration Number : 217MF10538
Registrant's Address : 5253 Okiube, Ube City, Yamaguchi Prefecture
Initial Date of Registration : 2005-09-09
Latest Date of Registration : 2010-02-23
Registration Number : 231MF10009
Registrant's Address : No. 7, Kunlunshan Road, Economic and Technological Development Zone, Lianyungang, Jia...
Initial Date of Registration : 2019-01-10
Latest Date of Registration : 2019-01-10
A Sevoflurane manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sevoflurane, including repackagers and relabelers. The FDA regulates Sevoflurane manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sevoflurane 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 Sevoflurane manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sevoflurane supplier is an individual or a company that provides Sevoflurane active pharmaceutical ingredient (API) or Sevoflurane finished formulations upon request. The Sevoflurane suppliers may include Sevoflurane API manufacturers, exporters, distributors and traders.
click here to find a list of Sevoflurane 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 Sevoflurane Drug Master File in Japan (Sevoflurane JDMF) empowers Sevoflurane 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 Sevoflurane JDMF during the approval evaluation for pharmaceutical products. At the time of Sevoflurane 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 Sevoflurane suppliers with JDMF on PharmaCompass.
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