Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
01 1CU CHEMIE UETIKON GMBH
01 1KETAMINE HYDROCHLORIDE
01 1France
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
Registration Number : 218MF10980
Registrant's Address : Raiffeisenstrasse 4, D-77933 Lahr Germany
Initial Date of Registration : 2006-12-01
Latest Date of Registration : 2021-12-09
A Ketamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ketamine, including repackagers and relabelers. The FDA regulates Ketamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ketamine 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 Ketamine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ketamine supplier is an individual or a company that provides Ketamine active pharmaceutical ingredient (API) or Ketamine finished formulations upon request. The Ketamine suppliers may include Ketamine API manufacturers, exporters, distributors and traders.
click here to find a list of Ketamine 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 Ketamine Drug Master File in Japan (Ketamine JDMF) empowers Ketamine 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 Ketamine JDMF during the approval evaluation for pharmaceutical products. At the time of Ketamine 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 Ketamine suppliers with JDMF on PharmaCompass.
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