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