Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1MOEHS IBERICA S. L.
02 1Edmond Pharma s. r. l.
03 1XINHE YUANSHENG MEDICINE CO. , LTD.
04 2Zhejiang East Asia Pharmaceutical Co. , Ltd.
01 2TRIMEBUTINE MALEATE
02 3Trimebutine maleate
01 3China
02 1Spain
03 1Sweden
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Registration Number : 226MF10117
Registrant's Address : Cesar Martinell i Brunet 12A, Poligono Rubi Sur, Rubi (Barcelona), Spain
Initial Date of Registration : 2014-06-18
Latest Date of Registration : 2023-03-07
Registration Number : 222MF10141
Registrant's Address : Via G. B. Grassi 15-20157 Milano Italy
Initial Date of Registration : 2010-04-20
Latest Date of Registration : 2010-04-20
Registration Number : 221MF10192
Registrant's Address : No. 185 East Liaocheng Road, Gushi County, Henan, China
Initial Date of Registration : 2009-08-18
Latest Date of Registration : 2009-08-18
Registration Number : 229MF10044
Registrant's Address : 23rd Floor, Chamber of Commerce Building North Laodong Road, Huangyan, Zhejiang, Chin...
Initial Date of Registration : 2017-02-20
Latest Date of Registration : 2024-10-16
Registration Number : 219MF10280
Registrant's Address : 23rd Floor, Chamber of Commerce Building North Laodong Road, Huangyan, Zhejiang, Chin...
Initial Date of Registration : 2007-09-10
Latest Date of Registration : 2011-01-07
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A Trimebutine Maleate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trimebutine Maleate, including repackagers and relabelers. The FDA regulates Trimebutine Maleate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trimebutine Maleate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Trimebutine Maleate supplier is an individual or a company that provides Trimebutine Maleate active pharmaceutical ingredient (API) or Trimebutine Maleate finished formulations upon request. The Trimebutine Maleate suppliers may include Trimebutine Maleate API manufacturers, exporters, distributors and traders.
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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 Trimebutine Maleate Drug Master File in Japan (Trimebutine Maleate JDMF) empowers Trimebutine Maleate 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 Trimebutine Maleate JDMF during the approval evaluation for pharmaceutical products. At the time of Trimebutine Maleate 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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