01 2Hovione PharmaScience Limited
02 1Zhejiang Hisun Pharmaceutical Co. , Ltd.
01 3Ivermectin
01 1China
02 2Portugal
Registration Number : 304MF10006
Registrant's Address : Estrada Coronel Nicolau de Mesquita Taipa, Macau S. A. R. China
Initial Date of Registration : 2022-01-11
Latest Date of Registration : 2022-01-11
Registration Number : 221MF10281
Registrant's Address : Estrada Coronel Nicolau de Mesquita Taipa, Macau S. A. R. China
Initial Date of Registration : 2009-12-18
Latest Date of Registration : 2021-10-07
Registration Number : 304MF10048
Registrant's Address : 46 Waisha Road, Jiaojiang District, Taizhou City, Zhejiang Province, P. R. China 3180...
Initial Date of Registration : 2022-03-02
Latest Date of Registration : 2022-03-02
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PharmaCompass offers a list of Ivermectin 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 Ivermectin manufacturer or Ivermectin supplier for your needs.
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A Ivermectin Merck Brand manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ivermectin Merck Brand, including repackagers and relabelers. The FDA regulates Ivermectin Merck Brand manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ivermectin Merck Brand 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 Ivermectin Merck Brand supplier is an individual or a company that provides Ivermectin Merck Brand active pharmaceutical ingredient (API) or Ivermectin Merck Brand finished formulations upon request. The Ivermectin Merck Brand suppliers may include Ivermectin Merck Brand 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 Ivermectin Merck Brand Drug Master File in Japan (Ivermectin Merck Brand JDMF) empowers Ivermectin Merck Brand 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 Ivermectin Merck Brand JDMF during the approval evaluation for pharmaceutical products. At the time of Ivermectin Merck Brand 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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