01 1Biocon Limited
02 1Boehringer Ingelheim Pharma GmbH & Co. K.G.
03 1Zhejiang Hisoar Chuannan Pharmaceutical Co. , Ltd.
01 3Repaglinide
01 1China
02 1Germany
03 1India
Registration Number : 231MF10044
Registrant's Address : 20th KM, Hosur Road, Electronics City-560100, Bengaluru, India
Initial Date of Registration : 2019-02-13
Latest Date of Registration : 2019-02-13
Registration Number : 221MF10144
Registrant's Address : Binger Strasse 173,55216 Ingelheim am Rhein
Initial Date of Registration : 2009-07-09
Latest Date of Registration : 2017-05-16
Registration Number : 306MF10117
Registrant's Address : No. 23,5th Donghai Avenue Zhejiang Chemical materials base Linhai zone, Linhai City, ...
Initial Date of Registration : 2024-08-28
Latest Date of Registration : 2024-08-28
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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 NovoNorm manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NovoNorm, including repackagers and relabelers. The FDA regulates NovoNorm manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NovoNorm 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 NovoNorm manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A NovoNorm supplier is an individual or a company that provides NovoNorm active pharmaceutical ingredient (API) or NovoNorm finished formulations upon request. The NovoNorm suppliers may include NovoNorm API manufacturers, exporters, distributors and traders.
click here to find a list of NovoNorm 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 NovoNorm Drug Master File in Japan (NovoNorm JDMF) empowers NovoNorm 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 NovoNorm JDMF during the approval evaluation for pharmaceutical products. At the time of NovoNorm 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 NovoNorm suppliers with JDMF on PharmaCompass.
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