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01 Japan Micro Biopharma Co., Ltd. (1)
01 Day stations josamycin (1)
01 Japan (1)
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PharmaCompass offers a list of Josamycin 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 Josamycin manufacturer or Josamycin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Josamycin manufacturer or Josamycin supplier.
PharmaCompass also assists you with knowing the Josamycin API Price utilized in the formulation of products. Josamycin API Price is not always fixed or binding as the Josamycin Price is obtained through a variety of data sources. The Josamycin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 11033-18-4 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 11033-18-4, including repackagers and relabelers. The FDA regulates 11033-18-4 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 11033-18-4 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 11033-18-4 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 11033-18-4 supplier is an individual or a company that provides 11033-18-4 active pharmaceutical ingredient (API) or 11033-18-4 finished formulations upon request. The 11033-18-4 suppliers may include 11033-18-4 API manufacturers, exporters, distributors and traders.
click here to find a list of 11033-18-4 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 11033-18-4 Drug Master File in Japan (11033-18-4 JDMF) empowers 11033-18-4 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 11033-18-4 JDMF during the approval evaluation for pharmaceutical products. At the time of 11033-18-4 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 11033-18-4 suppliers with JDMF on PharmaCompass.
We have 1 companies offering 11033-18-4
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