With Fermion, start the journey of your innovative API.
01 1Fermion Oy
02 1CHONGQING KANGLE PHARMACEUTICAL CO. , LTD.
01 2Hydroxychloroquine Sulfate
01 1China
02 1Finland
With Fermion, start the journey of your innovative API.
Registration Number : 305MF10090
Registrant's Address : Koivu-Mankkaan tie 6A, FI-02200 Espoo, Finland
Initial Date of Registration : 2023-08-02
Latest Date of Registration : 2023-08-02
Registration Number : 305MF10077
Registrant's Address : No. 4 HUAZHONG ROAD, CHONGQING (CHANGSHOU) CHEMICAL INDUSTRIAL PARK
Initial Date of Registration : 2023-07-05
Latest Date of Registration : 2023-07-05
A Hydroxychloroquine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hydroxychloroquine, including repackagers and relabelers. The FDA regulates Hydroxychloroquine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hydroxychloroquine 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 Hydroxychloroquine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hydroxychloroquine supplier is an individual or a company that provides Hydroxychloroquine active pharmaceutical ingredient (API) or Hydroxychloroquine finished formulations upon request. The Hydroxychloroquine suppliers may include Hydroxychloroquine API manufacturers, exporters, distributors and traders.
click here to find a list of Hydroxychloroquine 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 Hydroxychloroquine Drug Master File in Japan (Hydroxychloroquine JDMF) empowers Hydroxychloroquine 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 Hydroxychloroquine JDMF during the approval evaluation for pharmaceutical products. At the time of Hydroxychloroquine JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Hydroxychloroquine suppliers with JDMF on PharmaCompass.
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