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 : 2025-10-15
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
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A Selecor manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Selecor, including repackagers and relabelers. The FDA regulates Selecor manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Selecor 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 Selecor manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Selecor supplier is an individual or a company that provides Selecor active pharmaceutical ingredient (API) or Selecor finished formulations upon request. The Selecor suppliers may include Selecor API manufacturers, exporters, distributors and traders.
click here to find a list of Selecor 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 Selecor Drug Master File in Japan (Selecor JDMF) empowers Selecor 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 Selecor JDMF during the approval evaluation for pharmaceutical products. At the time of Selecor JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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