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01 Hokuko Chemical Industry Co., Ltd. (1)
01 Japanese Pharmacopoeia meticrane (production only) (1)
01 Japan (1)
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PharmaCompass offers a list of Meticrane 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 Meticrane manufacturer or Meticrane supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Meticrane manufacturer or Meticrane supplier.
PharmaCompass also assists you with knowing the Meticrane API Price utilized in the formulation of products. Meticrane API Price is not always fixed or binding as the Meticrane Price is obtained through a variety of data sources. The Meticrane Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MolPort-002-070-500 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-002-070-500, including repackagers and relabelers. The FDA regulates MolPort-002-070-500 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-002-070-500 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A MolPort-002-070-500 supplier is an individual or a company that provides MolPort-002-070-500 active pharmaceutical ingredient (API) or MolPort-002-070-500 finished formulations upon request. The MolPort-002-070-500 suppliers may include MolPort-002-070-500 API manufacturers, exporters, distributors and traders.
click here to find a list of MolPort-002-070-500 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 MolPort-002-070-500 Drug Master File in Japan (MolPort-002-070-500 JDMF) empowers MolPort-002-070-500 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 MolPort-002-070-500 JDMF during the approval evaluation for pharmaceutical products. At the time of MolPort-002-070-500 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 MolPort-002-070-500 suppliers with JDMF on PharmaCompass.
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