01 1Daito Co., Ltd.
02 1ESTECHPHARMA CO. , LTD.
03 1INIST ST CO. , LTD.
04 1Ipca Laboratories Limited
05 1Permakem Asia Co., Ltd.
06 1Polaris AI Pharma Corp.
07 1Shandong Xinhua Pharmaceutical Co. , Ltd.
08 1USV Private Limited
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PharmaCompass offers a list of Glimepiride 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 Glimepiride manufacturer or Glimepiride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Glimepiride manufacturer or Glimepiride supplier.
PharmaCompass also assists you with knowing the Glimepiride API Price utilized in the formulation of products. Glimepiride API Price is not always fixed or binding as the Glimepiride Price is obtained through a variety of data sources. The Glimepiride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Solosa manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Solosa, including repackagers and relabelers. The FDA regulates Solosa manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Solosa 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 Solosa manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Solosa supplier is an individual or a company that provides Solosa active pharmaceutical ingredient (API) or Solosa finished formulations upon request. The Solosa suppliers may include Solosa API manufacturers, exporters, distributors and traders.
click here to find a list of Solosa 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 Solosa Drug Master File in Japan (Solosa JDMF) empowers Solosa 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 Solosa JDMF during the approval evaluation for pharmaceutical products. At the time of Solosa 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 Solosa suppliers with JDMF on PharmaCompass.
We have 7 companies offering Solosa
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