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 Quilonorm manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Quilonorm, including repackagers and relabelers. The FDA regulates Quilonorm manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Quilonorm 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 Quilonorm manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Quilonorm supplier is an individual or a company that provides Quilonorm active pharmaceutical ingredient (API) or Quilonorm finished formulations upon request. The Quilonorm suppliers may include Quilonorm API manufacturers, exporters, distributors and traders.
click here to find a list of Quilonorm 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 Quilonorm Drug Master File in Japan (Quilonorm JDMF) empowers Quilonorm 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 Quilonorm JDMF during the approval evaluation for pharmaceutical products. At the time of Quilonorm 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 Quilonorm suppliers with JDMF on PharmaCompass.
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