01 1Novartis Pharmaceutical Manufacturing LLC
01 1Lithium carbonate
01 1Slovenia
Registration Number : 217MF10493
Registrant's Address : Verovskova ulica 57, 1000 Ljubljana, Slovenia
Initial Date of Registration : 2005-09-06
Latest Date of Registration : 2007-05-15
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PharmaCompass offers a list of Lithium Carbonate 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 Lithium Carbonate manufacturer or Lithium Carbonate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lithium Carbonate manufacturer or Lithium Carbonate supplier.
PharmaCompass also assists you with knowing the Lithium Carbonate API Price utilized in the formulation of products. Lithium Carbonate API Price is not always fixed or binding as the Lithium Carbonate Price is obtained through a variety of data sources. The Lithium Carbonate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Quilonum manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Quilonum, including repackagers and relabelers. The FDA regulates Quilonum manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Quilonum 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 Quilonum manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Quilonum supplier is an individual or a company that provides Quilonum active pharmaceutical ingredient (API) or Quilonum finished formulations upon request. The Quilonum suppliers may include Quilonum API manufacturers, exporters, distributors and traders.
click here to find a list of Quilonum 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 Quilonum Drug Master File in Japan (Quilonum JDMF) empowers Quilonum 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 Quilonum JDMF during the approval evaluation for pharmaceutical products. At the time of Quilonum 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 Quilonum suppliers with JDMF on PharmaCompass.
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