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 Sulphate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hydroxychloroquine Sulphate, including repackagers and relabelers. The FDA regulates Hydroxychloroquine Sulphate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hydroxychloroquine Sulphate 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 Sulphate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hydroxychloroquine Sulphate supplier is an individual or a company that provides Hydroxychloroquine Sulphate active pharmaceutical ingredient (API) or Hydroxychloroquine Sulphate finished formulations upon request. The Hydroxychloroquine Sulphate suppliers may include Hydroxychloroquine Sulphate API manufacturers, exporters, distributors and traders.
click here to find a list of Hydroxychloroquine Sulphate 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 Sulphate Drug Master File in Japan (Hydroxychloroquine Sulphate JDMF) empowers Hydroxychloroquine Sulphate 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 Sulphate JDMF during the approval evaluation for pharmaceutical products. At the time of Hydroxychloroquine Sulphate 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 Sulphate suppliers with JDMF on PharmaCompass.
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