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
A Vecuronium Bromide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vecuronium Bromide, including repackagers and relabelers. The FDA regulates Vecuronium Bromide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vecuronium Bromide 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 Vecuronium Bromide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Vecuronium Bromide supplier is an individual or a company that provides Vecuronium Bromide active pharmaceutical ingredient (API) or Vecuronium Bromide finished formulations upon request. The Vecuronium Bromide suppliers may include Vecuronium Bromide API manufacturers, exporters, distributors and traders.
click here to find a list of Vecuronium Bromide 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 Vecuronium Bromide Drug Master File in Japan (Vecuronium Bromide JDMF) empowers Vecuronium Bromide 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 Vecuronium Bromide JDMF during the approval evaluation for pharmaceutical products. At the time of Vecuronium Bromide 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 Vecuronium Bromide suppliers with JDMF on PharmaCompass.
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