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
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PharmaCompass offers a list of Sevoflurane 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 Sevoflurane manufacturer or Sevoflurane supplier for your needs.
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PharmaCompass also assists you with knowing the Sevoflurane API Price utilized in the formulation of products. Sevoflurane API Price is not always fixed or binding as the Sevoflurane Price is obtained through a variety of data sources. The Sevoflurane Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sojourn, Ultane, Sevorane manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sojourn, Ultane, Sevorane, including repackagers and relabelers. The FDA regulates Sojourn, Ultane, Sevorane manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sojourn, Ultane, Sevorane API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Sojourn, Ultane, Sevorane supplier is an individual or a company that provides Sojourn, Ultane, Sevorane active pharmaceutical ingredient (API) or Sojourn, Ultane, Sevorane finished formulations upon request. The Sojourn, Ultane, Sevorane suppliers may include Sojourn, Ultane, Sevorane API manufacturers, exporters, distributors and traders.
click here to find a list of Sojourn, Ultane, Sevorane 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 Sojourn, Ultane, Sevorane Drug Master File in Japan (Sojourn, Ultane, Sevorane JDMF) empowers Sojourn, Ultane, Sevorane 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 Sojourn, Ultane, Sevorane JDMF during the approval evaluation for pharmaceutical products. At the time of Sojourn, Ultane, Sevorane 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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