Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
01 1PCAS
01 1Piperidoreto hydrochloride
01 1France
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
Registration Number : 221MF10191
Registrant's Address : 21 chemin de la Sauvegarde, 21 Ecully Parc CS 33167 69134 Ecully Cedex FRANCE
Initial Date of Registration : 2009-08-18
Latest Date of Registration : 2009-08-18
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PharmaCompass offers a list of Piperidolate Hydrochloride 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 Piperidolate Hydrochloride manufacturer or Piperidolate Hydrochloride supplier for your needs.
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A Dactil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dactil, including repackagers and relabelers. The FDA regulates Dactil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dactil 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 Dactil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Dactil supplier is an individual or a company that provides Dactil active pharmaceutical ingredient (API) or Dactil finished formulations upon request. The Dactil suppliers may include Dactil API manufacturers, exporters, distributors and traders.
click here to find a list of Dactil 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 Dactil Drug Master File in Japan (Dactil JDMF) empowers Dactil 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 Dactil JDMF during the approval evaluation for pharmaceutical products. At the time of Dactil 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 Dactil suppliers with JDMF on PharmaCompass.
