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