01 1Guangdong Xianqiang Pharmaceutical Co. , Ltd.
01 1Pranoprofen
01 1Blank
Registration Number : 306MF10001
Registrant's Address : No. 6 Gongye Street, High-tech Economic Development Zone, Conghua, Guangzhou, Guangdo...
Initial Date of Registration : 2024-01-11
Latest Date of Registration : 2024-01-11
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A Pranoprofen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pranoprofen, including repackagers and relabelers. The FDA regulates Pranoprofen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pranoprofen 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 Pranoprofen manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Pranoprofen supplier is an individual or a company that provides Pranoprofen active pharmaceutical ingredient (API) or Pranoprofen finished formulations upon request. The Pranoprofen suppliers may include Pranoprofen API manufacturers, exporters, distributors and traders.
click here to find a list of Pranoprofen 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 Pranoprofen Drug Master File in Japan (Pranoprofen JDMF) empowers Pranoprofen 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 Pranoprofen JDMF during the approval evaluation for pharmaceutical products. At the time of Pranoprofen 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 Pranoprofen suppliers with JDMF on PharmaCompass.
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