Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
01 1PCAS
01 1Piperidoreto hydrochloride
01 1France
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
Registration Number : 221MF10191
Registrant's Address : 23, rue Bossuet Z. I. de la Vigne aux Loups F-91160 LONGJUMEAU France
Initial Date of Registration : 2009-08-18
Latest Date of Registration : 2009-08-18
A Piperidolate Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Piperidolate Hydrochloride, including repackagers and relabelers. The FDA regulates Piperidolate Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Piperidolate Hydrochloride 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 Piperidolate Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Piperidolate Hydrochloride supplier is an individual or a company that provides Piperidolate Hydrochloride active pharmaceutical ingredient (API) or Piperidolate Hydrochloride finished formulations upon request. The Piperidolate Hydrochloride suppliers may include Piperidolate Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Piperidolate Hydrochloride 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 Piperidolate Hydrochloride Drug Master File in Japan (Piperidolate Hydrochloride JDMF) empowers Piperidolate Hydrochloride 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 Piperidolate Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Piperidolate Hydrochloride 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 Piperidolate Hydrochloride suppliers with JDMF on PharmaCompass.
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