SCI Pharmtech offers high-quality, cost-effective APIs, advanced intermediates, & custom products with global expertise and precision.
01 1SCI Pharmtech, Inc.
02 1Anjan Drug Private Limited
03 1Mitsubishi Chemical Corporation
01 1Valproic Acid
02 2Valproic acid
01 1India
02 1Japan
03 1Taiwan
SCI Pharmtech offers high-quality, cost-effective APIs, advanced intermediates, & custom products with global expertise and precision.
Registration Number : 220MF10111
Registrant's Address : No. 61, Ln. 309, Haihu N. Rd. , Luzhu Dist. , Taoyuan City 33856, Taiwan
Initial Date of Registration : 2008-04-21
Latest Date of Registration : 2008-04-21
Registration Number : 303MF10181
Registrant's Address : 5th floor, Nelson Towers II wing, 117, Nelson Manickam Road, Aminjikarai, Chennai - 6...
Initial Date of Registration : 2021-12-15
Latest Date of Registration : 2021-12-15
Registration Number : 218MF10601
Registrant's Address : 1-1-1 Marunouchi, Chiyoda-ku, Tokyo
Initial Date of Registration : 2006-06-22
Latest Date of Registration : 2006-06-22
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PharmaCompass offers a list of Divalproex Sodium 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 Divalproex Sodium manufacturer or Divalproex Sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Divalproex Sodium manufacturer or Divalproex Sodium supplier.
PharmaCompass also assists you with knowing the Divalproex Sodium API Price utilized in the formulation of products. Divalproex Sodium API Price is not always fixed or binding as the Divalproex Sodium Price is obtained through a variety of data sources. The Divalproex Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Valproate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Valproate, including repackagers and relabelers. The FDA regulates Valproate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Valproate 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 Valproate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Valproate supplier is an individual or a company that provides Valproate active pharmaceutical ingredient (API) or Valproate finished formulations upon request. The Valproate suppliers may include Valproate API manufacturers, exporters, distributors and traders.
click here to find a list of Valproate 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 Valproate Drug Master File in Japan (Valproate JDMF) empowers Valproate 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 Valproate JDMF during the approval evaluation for pharmaceutical products. At the time of Valproate 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 Valproate suppliers with JDMF on PharmaCompass.
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