Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1MOEHS IBERICA S. L.
02 1MOEHS IBERICA, S. L.
01 2CELIPROLOL HYDROCHLORIDE
01 2Spain
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Registration Number : 230MF10051
Registrant's Address : Cesar Martinell i Brunet 12A, Poligono Rubi Sur, Rubi (Barcelona), Spain
Initial Date of Registration : 2018-04-09
Latest Date of Registration : 2021-08-16
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Registration Number : 219MF10204
Registrant's Address : Cesar Martinell i Brunet 12A, Poligono Rubi Sur, Rubi (Barcelona), Spain
Initial Date of Registration : 2007-06-13
Latest Date of Registration : 2007-06-13
A Celiprolol Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Celiprolol Hydrochloride, including repackagers and relabelers. The FDA regulates Celiprolol Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Celiprolol 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 Celiprolol Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Celiprolol Hydrochloride supplier is an individual or a company that provides Celiprolol Hydrochloride active pharmaceutical ingredient (API) or Celiprolol Hydrochloride finished formulations upon request. The Celiprolol Hydrochloride suppliers may include Celiprolol Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Celiprolol 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 Celiprolol Hydrochloride Drug Master File in Japan (Celiprolol Hydrochloride JDMF) empowers Celiprolol 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 Celiprolol Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Celiprolol 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 Celiprolol Hydrochloride suppliers with JDMF on PharmaCompass.
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