01 1Henan Quanyu Pharmaceutical Co. , Ltd.
01 1Tiopronin
01 1China
Registration Number : 303MF10092
Registrant's Address : Industrial Park, Neixiang County, Nanyang City, Henan, China
Initial Date of Registration : 2021-06-09
Latest Date of Registration : 2021-06-09
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PharmaCompass offers a list of Tiopronin 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 Tiopronin manufacturer or Tiopronin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tiopronin manufacturer or Tiopronin supplier.
PharmaCompass also assists you with knowing the Tiopronin API Price utilized in the formulation of products. Tiopronin API Price is not always fixed or binding as the Tiopronin Price is obtained through a variety of data sources. The Tiopronin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A THIOLA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of THIOLA, including repackagers and relabelers. The FDA regulates THIOLA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. THIOLA 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 THIOLA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A THIOLA supplier is an individual or a company that provides THIOLA active pharmaceutical ingredient (API) or THIOLA finished formulations upon request. The THIOLA suppliers may include THIOLA API manufacturers, exporters, distributors and traders.
click here to find a list of THIOLA 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 THIOLA Drug Master File in Japan (THIOLA JDMF) empowers THIOLA 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 THIOLA JDMF during the approval evaluation for pharmaceutical products. At the time of THIOLA 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 THIOLA suppliers with JDMF on PharmaCompass.
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