01 1Daito Co., Ltd.
01 1Day stations pindolol (production only)
01 1Japan
JP Pindolol (for manufacturing only)
Registration Number : 217MF10627
Registrant's Address : 326 Yokamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2005-09-29
Latest Date of Registration : 2006-08-23
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PharmaCompass offers a list of Pindolol 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 Pindolol manufacturer or Pindolol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pindolol manufacturer or Pindolol supplier.
PharmaCompass also assists you with knowing the Pindolol API Price utilized in the formulation of products. Pindolol API Price is not always fixed or binding as the Pindolol Price is obtained through a variety of data sources. The Pindolol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Visken manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Visken, including repackagers and relabelers. The FDA regulates Visken manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Visken 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 Visken manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Visken supplier is an individual or a company that provides Visken active pharmaceutical ingredient (API) or Visken finished formulations upon request. The Visken suppliers may include Visken API manufacturers, exporters, distributors and traders.
click here to find a list of Visken 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 Visken Drug Master File in Japan (Visken JDMF) empowers Visken 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 Visken JDMF during the approval evaluation for pharmaceutical products. At the time of Visken 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 Visken suppliers with JDMF on PharmaCompass.
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