01 1Siegfried Evionnaz SA
01 1Tetracaine hydrochloride Tetracaine Hydrochloride
01 1Switzerland
Registration Number : 220MF10198
Registrant's Address : Route du Simplon 1,36,CH-1902 Evionnaz,Switzerland
Initial Date of Registration : 2008-09-09
Latest Date of Registration : 2024-06-27
A Tetracaine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tetracaine Hydrochloride, including repackagers and relabelers. The FDA regulates Tetracaine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tetracaine 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 Tetracaine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tetracaine Hydrochloride supplier is an individual or a company that provides Tetracaine Hydrochloride active pharmaceutical ingredient (API) or Tetracaine Hydrochloride finished formulations upon request. The Tetracaine Hydrochloride suppliers may include Tetracaine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Tetracaine 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 Tetracaine Hydrochloride Drug Master File in Japan (Tetracaine Hydrochloride JDMF) empowers Tetracaine 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 Tetracaine Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Tetracaine 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 Tetracaine Hydrochloride suppliers with JDMF on PharmaCompass.
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