01 1INIST ST CO. , LTD.
01 1Pioglitazone
01 1South Korea
Registration Number : 222MF10077
Registrant's Address : 500, Sinnae-ro, Geumwang-eup, Eumseong-gun, Chungcheongbuk-do, Korea
Initial Date of Registration : 2010-03-02
Latest Date of Registration : 2010-03-02
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PharmaCompass offers a list of Pioglitazone 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 Pioglitazone manufacturer or Pioglitazone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pioglitazone manufacturer or Pioglitazone supplier.
PharmaCompass also assists you with knowing the Pioglitazone API Price utilized in the formulation of products. Pioglitazone API Price is not always fixed or binding as the Pioglitazone Price is obtained through a variety of data sources. The Pioglitazone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Glustin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glustin, including repackagers and relabelers. The FDA regulates Glustin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glustin 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 Glustin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Glustin supplier is an individual or a company that provides Glustin active pharmaceutical ingredient (API) or Glustin finished formulations upon request. The Glustin suppliers may include Glustin API manufacturers, exporters, distributors and traders.
click here to find a list of Glustin 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 Glustin Drug Master File in Japan (Glustin JDMF) empowers Glustin 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 Glustin JDMF during the approval evaluation for pharmaceutical products. At the time of Glustin 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 Glustin suppliers with JDMF on PharmaCompass.
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