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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PharmaCompass offers a list of Trimebutine Maleate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Trimebutine Maleate manufacturer or Trimebutine Maleate supplier for your needs.
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A Trimebutine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trimebutine, including repackagers and relabelers. The FDA regulates Trimebutine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trimebutine 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 supplier is an individual or a company that provides Trimebutine active pharmaceutical ingredient (API) or Trimebutine finished formulations upon request. The Trimebutine suppliers may include Trimebutine 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 Drug Master File in Japan (Trimebutine JDMF) empowers Trimebutine 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 JDMF during the approval evaluation for pharmaceutical products. At the time of Trimebutine 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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