Registration Number : 222MF10223
Registrant's Address : Great Eastern Chambers, CBD Belapur, Navi Mumbai-400 614, India
Initial Date of Registration : 2010-09-03
Latest Date of Registration : 2013-01-18
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PharmaCompass offers a list of Gabapentin 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 Gabapentin manufacturer or Gabapentin supplier for your needs.
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PharmaCompass also assists you with knowing the Gabapentin API Price utilized in the formulation of products. Gabapentin API Price is not always fixed or binding as the Gabapentin Price is obtained through a variety of data sources. The Gabapentin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DM-1796 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DM-1796, including repackagers and relabelers. The FDA regulates DM-1796 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DM-1796 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A DM-1796 supplier is an individual or a company that provides DM-1796 active pharmaceutical ingredient (API) or DM-1796 finished formulations upon request. The DM-1796 suppliers may include DM-1796 API manufacturers, exporters, distributors and traders.
click here to find a list of DM-1796 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 DM-1796 Drug Master File in Japan (DM-1796 JDMF) empowers DM-1796 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 DM-1796 JDMF during the approval evaluation for pharmaceutical products. At the time of DM-1796 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 DM-1796 suppliers with JDMF on PharmaCompass.
