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