IKF/Pharmasynthese have been with fine chemicals market and APIs performance for more than 40 years.
01 1Pharmasynthesis SAS
01 1Day stations Torepibuton (production only)
01 1France
IKF/Pharmasynthese have been with fine chemicals market and APIs performance for more than 40 years.
JP Trepibutone (for manufacturing only)
Registration Number : 223MF10168
Registrant's Address : 57, rue Gravetel St Pierre Les Elbeuf France
Initial Date of Registration : 2011-12-09
Latest Date of Registration : 2011-12-09
A Trepibutone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trepibutone, including repackagers and relabelers. The FDA regulates Trepibutone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trepibutone 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 Trepibutone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Trepibutone supplier is an individual or a company that provides Trepibutone active pharmaceutical ingredient (API) or Trepibutone finished formulations upon request. The Trepibutone suppliers may include Trepibutone API manufacturers, exporters, distributors and traders.
click here to find a list of Trepibutone 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 Trepibutone Drug Master File in Japan (Trepibutone JDMF) empowers Trepibutone 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 Trepibutone JDMF during the approval evaluation for pharmaceutical products. At the time of Trepibutone 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 Trepibutone suppliers with JDMF on PharmaCompass.
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