01 1Xellia Pharmaceuticals Ltd.
01 1Gramicidin
01 1Denmark
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, Price,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.
PharmaCompass also assists you with knowing the Gramicidin API Price utilized in the formulation of products. Gramicidin API Price is not always fixed or binding as the Gramicidin Price is obtained through a variety of data sources. The Gramicidin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Gramicidina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gramicidina, including repackagers and relabelers. The FDA regulates Gramicidina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gramicidina 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 Gramicidina manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Gramicidina supplier is an individual or a company that provides Gramicidina active pharmaceutical ingredient (API) or Gramicidina finished formulations upon request. The Gramicidina suppliers may include Gramicidina API manufacturers, exporters, distributors and traders.
click here to find a list of Gramicidina 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 Gramicidina Drug Master File in Japan (Gramicidina JDMF) empowers Gramicidina 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 Gramicidina JDMF during the approval evaluation for pharmaceutical products. At the time of Gramicidina 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 Gramicidina suppliers with JDMF on PharmaCompass.
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