01 1Siegfried Evionnaz SA
01 1Prilocaine Prilocaine
01 1Switzerland
Registration Number : 222MF10085
Registrant's Address : Route du Simplon 1,36,CH-1902 Evionnaz,Switzerland
Initial Date of Registration : 2010-03-16
Latest Date of Registration : 2016-12-07
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PharmaCompass offers a list of Prilocaine 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 Prilocaine manufacturer or Prilocaine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Prilocaine manufacturer or Prilocaine supplier.
PharmaCompass also assists you with knowing the Prilocaine API Price utilized in the formulation of products. Prilocaine API Price is not always fixed or binding as the Prilocaine Price is obtained through a variety of data sources. The Prilocaine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Takipril manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Takipril, including repackagers and relabelers. The FDA regulates Takipril manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Takipril 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 Takipril manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Takipril supplier is an individual or a company that provides Takipril active pharmaceutical ingredient (API) or Takipril finished formulations upon request. The Takipril suppliers may include Takipril API manufacturers, exporters, distributors and traders.
click here to find a list of Takipril 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 Takipril Drug Master File in Japan (Takipril JDMF) empowers Takipril 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 Takipril JDMF during the approval evaluation for pharmaceutical products. At the time of Takipril 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 Takipril suppliers with JDMF on PharmaCompass.
