01 1Kern Pharma, S. L.
01 1Remifentanil hydrochloride
01 1Spain
Registration Number : 226MF10170
Registrant's Address : Pol. Ind. Colo(´)n II Venus, 72 08228 Terrassa (Barcelona)-Spain
Initial Date of Registration : 2014-09-01
Latest Date of Registration : 2018-10-12
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PharmaCompass offers a list of Remifentanil API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Remifentanil manufacturer or Remifentanil supplier for your needs.
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A Remifentanil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Remifentanil, including repackagers and relabelers. The FDA regulates Remifentanil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Remifentanil 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 Remifentanil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Remifentanil supplier is an individual or a company that provides Remifentanil active pharmaceutical ingredient (API) or Remifentanil finished formulations upon request. The Remifentanil suppliers may include Remifentanil API manufacturers, exporters, distributors and traders.
click here to find a list of Remifentanil suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Remifentanil Drug Master File in Japan (Remifentanil JDMF) empowers Remifentanil 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 Remifentanil JDMF during the approval evaluation for pharmaceutical products. At the time of Remifentanil 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 Remifentanil suppliers with JDMF on PharmaCompass.
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