01 1Curia Italy S. r. l.
01 1Vecuronium bromide
01 1U.S.A
Registration Number : 218MF10989
Registrant's Address : Via del Vecchio Politecnico n. 9, 20121 Milano (MI) - Italy
Initial Date of Registration : 2006-12-18
Latest Date of Registration : 2018-11-07
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PharmaCompass offers a list of Vecuronium Bromide 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 Vecuronium Bromide manufacturer or Vecuronium Bromide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Vecuronium Bromide manufacturer or Vecuronium Bromide supplier.
PharmaCompass also assists you with knowing the Vecuronium Bromide API Price utilized in the formulation of products. Vecuronium Bromide API Price is not always fixed or binding as the Vecuronium Bromide Price is obtained through a variety of data sources. The Vecuronium Bromide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Norcuron manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Norcuron, including repackagers and relabelers. The FDA regulates Norcuron manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Norcuron 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 Norcuron manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Norcuron supplier is an individual or a company that provides Norcuron active pharmaceutical ingredient (API) or Norcuron finished formulations upon request. The Norcuron suppliers may include Norcuron API manufacturers, exporters, distributors and traders.
click here to find a list of Norcuron 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 Norcuron Drug Master File in Japan (Norcuron JDMF) empowers Norcuron 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 Norcuron JDMF during the approval evaluation for pharmaceutical products. At the time of Norcuron 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 Norcuron suppliers with JDMF on PharmaCompass.
