Registration Number : 306MF10012
Registrant's Address : Strada Rivoltana Km 6/7 20053 Rodano Milano Italy
Initial Date of Registration : 2024-01-17
Latest Date of Registration : 2024-01-17
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PharmaCompass offers a list of Artemether 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 Artemether manufacturer or Artemether supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Artemether manufacturer or Artemether supplier.
PharmaCompass also assists you with knowing the Artemether API Price utilized in the formulation of products. Artemether API Price is not always fixed or binding as the Artemether Price is obtained through a variety of data sources. The Artemether Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Malartem manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Malartem, including repackagers and relabelers. The FDA regulates Malartem manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Malartem 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 Malartem manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Malartem supplier is an individual or a company that provides Malartem active pharmaceutical ingredient (API) or Malartem finished formulations upon request. The Malartem suppliers may include Malartem API manufacturers, exporters, distributors and traders.
click here to find a list of Malartem 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 Malartem Drug Master File in Japan (Malartem JDMF) empowers Malartem 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 Malartem JDMF during the approval evaluation for pharmaceutical products. At the time of Malartem 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 Malartem suppliers with JDMF on PharmaCompass.
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