01 1NOBILUS ENT Tomasz Koz(')luk
01 1Deslanosid
01 1Poland
Registration Number : 230MF10104
Registrant's Address : ul. Swarzewska 45,01-821 Warszawa, POLAND
Initial Date of Registration : 2018-08-08
Latest Date of Registration : 2018-08-08
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PharmaCompass offers a list of Deslanoside 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 Deslanoside manufacturer or Deslanoside supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Deslanoside manufacturer or Deslanoside supplier.
PharmaCompass also assists you with knowing the Deslanoside API Price utilized in the formulation of products. Deslanoside API Price is not always fixed or binding as the Deslanoside Price is obtained through a variety of data sources. The Deslanoside Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cedilanid D manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cedilanid D, including repackagers and relabelers. The FDA regulates Cedilanid D manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cedilanid D 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 Cedilanid D manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cedilanid D supplier is an individual or a company that provides Cedilanid D active pharmaceutical ingredient (API) or Cedilanid D finished formulations upon request. The Cedilanid D suppliers may include Cedilanid D API manufacturers, exporters, distributors and traders.
click here to find a list of Cedilanid D 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 Cedilanid D Drug Master File in Japan (Cedilanid D JDMF) empowers Cedilanid D 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 Cedilanid D JDMF during the approval evaluation for pharmaceutical products. At the time of Cedilanid D 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 Cedilanid D suppliers with JDMF on PharmaCompass.
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