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
94
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 3ppp manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 3ppp, including repackagers and relabelers. The FDA regulates 3ppp manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 3ppp 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 3ppp manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 3ppp supplier is an individual or a company that provides 3ppp active pharmaceutical ingredient (API) or 3ppp finished formulations upon request. The 3ppp suppliers may include 3ppp API manufacturers, exporters, distributors and traders.
click here to find a list of 3ppp 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 3ppp Drug Master File in Japan (3ppp JDMF) empowers 3ppp 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 3ppp JDMF during the approval evaluation for pharmaceutical products. At the time of 3ppp 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 3ppp suppliers with JDMF on PharmaCompass.
