01 1Aurobindo Pharma Limited
02 1Ningbo Menovo Pharmaceutical Co. , Ltd.
03 1Oril Industry
04 2Permakem Asia Co., Ltd.
01 1Bae Lind erbumine
02 4Perindopril erbumine
01 1China
02 1France
03 1India
04 2Japan
Registration Number : 227MF10018
Registrant's Address : Plot No. 2, Maitrivihar, Ameerpet, Hyderabad Andhra Pradesh, India
Initial Date of Registration : 2015-01-05
Latest Date of Registration : 2015-01-05
Registration Number : 227MF10137
Registrant's Address : 12B/F, Building 1, Ningbo R&D Park, No 999, YangFan Rd. , Hi-Tech district, Ningbo 31...
Initial Date of Registration : 2015-05-14
Latest Date of Registration : 2017-05-19
Registration Number : 228MF10112
Registrant's Address : 1-10-11, Nihonbashi Horidomecho, Chuo-ku, Tokyo
Initial Date of Registration : 2016-06-10
Latest Date of Registration : 2016-06-10
Registration Number : 217MF11143
Registrant's Address : 7-6, Nihonbashi Odenmacho, Chuo-ku, Tokyo
Initial Date of Registration : 2005-12-05
Latest Date of Registration : 2007-03-05
Registration Number : 217MF10333
Registrant's Address : 13, rue Auguste Desgene(') tais, 76210 Bolbec, FRANCE
Initial Date of Registration : 2005-08-09
Latest Date of Registration : 2008-11-21
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PharmaCompass offers a list of Perindopril Erbumine 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 Perindopril Erbumine manufacturer or Perindopril Erbumine supplier for your needs.
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A Perindopril Erbumine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Perindopril Erbumine, including repackagers and relabelers. The FDA regulates Perindopril Erbumine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Perindopril Erbumine 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 Perindopril Erbumine supplier is an individual or a company that provides Perindopril Erbumine active pharmaceutical ingredient (API) or Perindopril Erbumine finished formulations upon request. The Perindopril Erbumine suppliers may include Perindopril Erbumine API manufacturers, exporters, distributors and traders.
click here to find a list of Perindopril Erbumine 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 Perindopril Erbumine Drug Master File in Japan (Perindopril Erbumine JDMF) empowers Perindopril Erbumine 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 Perindopril Erbumine JDMF during the approval evaluation for pharmaceutical products. At the time of Perindopril Erbumine 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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