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01 Biocon Limited (1)
02 Boehringer Ingelheim Pharma GmbH & Co. K.G. (1)
01 Repaglinide (2)
01 Germany (1)
02 India (1)
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PharmaCompass offers a list of Repaglinide 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 Repaglinide manufacturer or Repaglinide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Repaglinide manufacturer or Repaglinide supplier.
PharmaCompass also assists you with knowing the Repaglinide API Price utilized in the formulation of products. Repaglinide API Price is not always fixed or binding as the Repaglinide Price is obtained through a variety of data sources. The Repaglinide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Repaglinide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Repaglinide, including repackagers and relabelers. The FDA regulates Repaglinide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Repaglinide 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 Repaglinide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Repaglinide supplier is an individual or a company that provides Repaglinide active pharmaceutical ingredient (API) or Repaglinide finished formulations upon request. The Repaglinide suppliers may include Repaglinide API manufacturers, exporters, distributors and traders.
click here to find a list of Repaglinide 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 Repaglinide Drug Master File in Japan (Repaglinide JDMF) empowers Repaglinide 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 Repaglinide JDMF during the approval evaluation for pharmaceutical products. At the time of Repaglinide 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 Repaglinide suppliers with JDMF on PharmaCompass.
We have 2 companies offering Repaglinide
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