01 1MicroBiopharm Japan Co., Ltd.
01 1Day stations josamycin
01 1Japan
Registration Number : 217MF10599
Registrant's Address : 1-3-1 Kyobashi, Chuo-ku, Tokyo
Initial Date of Registration : 2005-09-14
Latest Date of Registration : 2010-01-28
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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 Leucomycin A3 (Kitasamycin component) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Leucomycin A3 (Kitasamycin component), including repackagers and relabelers. The FDA regulates Leucomycin A3 (Kitasamycin component) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Leucomycin A3 (Kitasamycin component) API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Leucomycin A3 (Kitasamycin component) supplier is an individual or a company that provides Leucomycin A3 (Kitasamycin component) active pharmaceutical ingredient (API) or Leucomycin A3 (Kitasamycin component) finished formulations upon request. The Leucomycin A3 (Kitasamycin component) suppliers may include Leucomycin A3 (Kitasamycin component) API manufacturers, exporters, distributors and traders.
click here to find a list of Leucomycin A3 (Kitasamycin component) 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 Leucomycin A3 (Kitasamycin component) Drug Master File in Japan (Leucomycin A3 (Kitasamycin component) JDMF) empowers Leucomycin A3 (Kitasamycin component) 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 Leucomycin A3 (Kitasamycin component) JDMF during the approval evaluation for pharmaceutical products. At the time of Leucomycin A3 (Kitasamycin component) 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 Leucomycin A3 (Kitasamycin component) suppliers with JDMF on PharmaCompass.
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