Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
01 1Wavelength Enterprises Ltd
02 1ScinoPharm Taiwan, Ltd.
03 1Synthon s. r. o.
01 3Flumazenil
01 1France
02 1Netherlands
03 1Taiwan
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
Registration Number : 218MF11004
Registrant's Address : Ofer Park, Brosh Building, 4th floor, 94 Shlomo Shmeltzer Road, POB 3158, Petah Tikva...
Initial Date of Registration : 2006-12-18
Latest Date of Registration : 2006-12-18
Registration Number : 228MF10180
Registrant's Address : No. 1, Nan-Ke 8th Road, Shan-Hua, Tainan 74144 Taiwan
Initial Date of Registration : 2016-09-08
Latest Date of Registration : 2016-09-08
Registration Number : 227MF10174
Registrant's Address : Brnenska 32, 678 17 Blansko, Czech Republic
Initial Date of Registration : 2015-06-26
Latest Date of Registration : 2015-06-26
A Flumazenil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flumazenil, including repackagers and relabelers. The FDA regulates Flumazenil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flumazenil 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 Flumazenil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Flumazenil supplier is an individual or a company that provides Flumazenil active pharmaceutical ingredient (API) or Flumazenil finished formulations upon request. The Flumazenil suppliers may include Flumazenil API manufacturers, exporters, distributors and traders.
click here to find a list of Flumazenil 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 Flumazenil Drug Master File in Japan (Flumazenil JDMF) empowers Flumazenil 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 Flumazenil JDMF during the approval evaluation for pharmaceutical products. At the time of Flumazenil 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 Flumazenil suppliers with JDMF on PharmaCompass.
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