01 1Siegfried Evionnaz SA
01 1Hydrochloric acid prilocaine
01 1Switzerland
Registration Number : 219MF10013
Registrant's Address : Route du Simplon 1,36,CH-1902 Evionnaz,Switzerland
Initial Date of Registration : 2007-01-18
Latest Date of Registration : 2022-05-25
A Prilocaine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prilocaine Hydrochloride, including repackagers and relabelers. The FDA regulates Prilocaine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prilocaine Hydrochloride 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 Prilocaine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Prilocaine Hydrochloride supplier is an individual or a company that provides Prilocaine Hydrochloride active pharmaceutical ingredient (API) or Prilocaine Hydrochloride finished formulations upon request. The Prilocaine Hydrochloride suppliers may include Prilocaine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Prilocaine Hydrochloride 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 Prilocaine Hydrochloride Drug Master File in Japan (Prilocaine Hydrochloride JDMF) empowers Prilocaine Hydrochloride 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 Prilocaine Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Prilocaine Hydrochloride 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 Prilocaine Hydrochloride suppliers with JDMF on PharmaCompass.
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