01 1piCHEM Forschungs- und Entwicklungs GmbH
01 1Daughter Octreotate (trifluoroacetic acid salt)
01 1Austria
Dotaoctreotate (trifluoroacetate)
Registration Number : 303MF10074
Registrant's Address : Parkring 3, 8074 Raaba-Grambach, Austria
Initial Date of Registration : 2021-04-27
Latest Date of Registration : 2022-08-03
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PharmaCompass offers a list of Trifluoroacetic Acid 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 Trifluoroacetic Acid manufacturer or Trifluoroacetic Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Trifluoroacetic Acid manufacturer or Trifluoroacetic Acid supplier.
PharmaCompass also assists you with knowing the Trifluoroacetic Acid API Price utilized in the formulation of products. Trifluoroacetic Acid API Price is not always fixed or binding as the Trifluoroacetic Acid Price is obtained through a variety of data sources. The Trifluoroacetic Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A TFA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of TFA, including repackagers and relabelers. The FDA regulates TFA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. TFA 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 TFA supplier is an individual or a company that provides TFA active pharmaceutical ingredient (API) or TFA finished formulations upon request. The TFA suppliers may include TFA API manufacturers, exporters, distributors and traders.
click here to find a list of TFA 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 TFA Drug Master File in Japan (TFA JDMF) empowers TFA 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 TFA JDMF during the approval evaluation for pharmaceutical products. At the time of TFA 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 TFA suppliers with JDMF on PharmaCompass.
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