Expand your portfolio with Egis- value-added generics, API capabilities, and reliable contract services to drive your growth.
01 1EGIS PHARMACEUTICALS PRIVATE LIMITED COMPANY
01 1Tofisopam
01 1Hungary
Expand your portfolio with Egis- value-added generics, API capabilities, and reliable contract services to drive your growth.
Registration Number : 219MF10297
Registrant's Address : H-1106 BUDAPEST KERESZTURI UT 30-38 HUNGARY
Initial Date of Registration : 2007-09-18
Latest Date of Registration : 2021-09-28
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PharmaCompass offers a list of Tofisopam API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Tofisopam manufacturer or Tofisopam supplier for your needs.
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A dextofisopam manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of dextofisopam, including repackagers and relabelers. The FDA regulates dextofisopam manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. dextofisopam 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 dextofisopam manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A dextofisopam supplier is an individual or a company that provides dextofisopam active pharmaceutical ingredient (API) or dextofisopam finished formulations upon request. The dextofisopam suppliers may include dextofisopam API manufacturers, exporters, distributors and traders.
click here to find a list of dextofisopam suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 dextofisopam Drug Master File in Japan (dextofisopam JDMF) empowers dextofisopam 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 dextofisopam JDMF during the approval evaluation for pharmaceutical products. At the time of dextofisopam 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 dextofisopam suppliers with JDMF on PharmaCompass.
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