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 Cosyntropin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cosyntropin, including repackagers and relabelers. The FDA regulates Cosyntropin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cosyntropin 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 Cosyntropin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cosyntropin supplier is an individual or a company that provides Cosyntropin active pharmaceutical ingredient (API) or Cosyntropin finished formulations upon request. The Cosyntropin suppliers may include Cosyntropin API manufacturers, exporters, distributors and traders.
click here to find a list of Cosyntropin 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 Cosyntropin Drug Master File in Japan (Cosyntropin JDMF) empowers Cosyntropin 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 Cosyntropin JDMF during the approval evaluation for pharmaceutical products. At the time of Cosyntropin 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 Cosyntropin suppliers with JDMF on PharmaCompass.
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