01 1AMINO GmbH
01 1Betaine anhydrous
01 1Germany
Registration Number : 225MF10183
Registrant's Address : An der Zucker-Raffinerie 9, 38373 Frellstedt, Germany
Initial Date of Registration : 2013-09-25
Latest Date of Registration : 2023-09-13
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PharmaCompass offers a list of Betaine 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 Betaine manufacturer or Betaine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Betaine manufacturer or Betaine supplier.
PharmaCompass also assists you with knowing the Betaine API Price utilized in the formulation of products. Betaine API Price is not always fixed or binding as the Betaine Price is obtained through a variety of data sources. The Betaine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Betafin BP manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Betafin BP, including repackagers and relabelers. The FDA regulates Betafin BP manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Betafin BP 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 Betafin BP supplier is an individual or a company that provides Betafin BP active pharmaceutical ingredient (API) or Betafin BP finished formulations upon request. The Betafin BP suppliers may include Betafin BP API manufacturers, exporters, distributors and traders.
click here to find a list of Betafin BP 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 Betafin BP Drug Master File in Japan (Betafin BP JDMF) empowers Betafin BP 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 Betafin BP JDMF during the approval evaluation for pharmaceutical products. At the time of Betafin BP JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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