01 1Lusochimica S. p. A.
01 1Sulfadiazine Silver
01 1Italy
Registration Number : 229MF10205
Registrant's Address : Via Giotto 9,23871 Lomagna(LC)Italy
Initial Date of Registration : 2017-11-21
Latest Date of Registration : 2019-12-10
A Silver Sulfadiazine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Silver Sulfadiazine, including repackagers and relabelers. The FDA regulates Silver Sulfadiazine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Silver Sulfadiazine 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 Silver Sulfadiazine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Silver Sulfadiazine supplier is an individual or a company that provides Silver Sulfadiazine active pharmaceutical ingredient (API) or Silver Sulfadiazine finished formulations upon request. The Silver Sulfadiazine suppliers may include Silver Sulfadiazine API manufacturers, exporters, distributors and traders.
click here to find a list of Silver Sulfadiazine 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 Silver Sulfadiazine Drug Master File in Japan (Silver Sulfadiazine JDMF) empowers Silver Sulfadiazine 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 Silver Sulfadiazine JDMF during the approval evaluation for pharmaceutical products. At the time of Silver Sulfadiazine 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 Silver Sulfadiazine suppliers with JDMF on PharmaCompass.
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