Xellia Delivering Reliable Anti-Infective Solutions Through Expertise, Quality, and Uninterrupted Global Supply.
01 1Xellia Pharmaceuticals Ltd.
01 1Gramicidin
01 1Denmark
Xellia Delivering Reliable Anti-Infective Solutions Through Expertise, Quality, and Uninterrupted Global Supply.
Registration Number : 218MF10936
Registrant's Address : H-1107 Budapest, Sza(´)lla(´)s u. 3. Hungary
Initial Date of Registration : 2006-11-21
Latest Date of Registration : 2006-11-21
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PharmaCompass offers a list of Gramicidin 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 Gramicidin manufacturer or Gramicidin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Gramicidin manufacturer or Gramicidin supplier.
A Gramicidinum [INN-Latin] manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gramicidinum [INN-Latin], including repackagers and relabelers. The FDA regulates Gramicidinum [INN-Latin] manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gramicidinum [INN-Latin] 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 Gramicidinum [INN-Latin] manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Gramicidinum [INN-Latin] supplier is an individual or a company that provides Gramicidinum [INN-Latin] active pharmaceutical ingredient (API) or Gramicidinum [INN-Latin] finished formulations upon request. The Gramicidinum [INN-Latin] suppliers may include Gramicidinum [INN-Latin] API manufacturers, exporters, distributors and traders.
click here to find a list of Gramicidinum [INN-Latin] 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 Gramicidinum [INN-Latin] Drug Master File in Japan (Gramicidinum [INN-Latin] JDMF) empowers Gramicidinum [INN-Latin] 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 Gramicidinum [INN-Latin] JDMF during the approval evaluation for pharmaceutical products. At the time of Gramicidinum [INN-Latin] 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 Gramicidinum [INN-Latin] suppliers with JDMF on PharmaCompass.
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