01 1BCN Peptides S. A.
01 1Tetracosactide
01 1Spain
Registration Number : 222MF10242
Registrant's Address : Poligono industrial Els Vinyets-Els Fogars. Sector II 08777-Sant Quinti de Mediona, B...
Initial Date of Registration : 2010-10-13
Latest Date of Registration : 2010-10-13
A Tetracosactide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tetracosactide, including repackagers and relabelers. The FDA regulates Tetracosactide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tetracosactide 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 Tetracosactide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tetracosactide supplier is an individual or a company that provides Tetracosactide active pharmaceutical ingredient (API) or Tetracosactide finished formulations upon request. The Tetracosactide suppliers may include Tetracosactide API manufacturers, exporters, distributors and traders.
click here to find a list of Tetracosactide 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 Tetracosactide Drug Master File in Japan (Tetracosactide JDMF) empowers Tetracosactide 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 Tetracosactide JDMF during the approval evaluation for pharmaceutical products. At the time of Tetracosactide 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 Tetracosactide suppliers with JDMF on PharmaCompass.
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