01 1UMICORE Argentina SA
01 1Lomustine
01 1Germany
Registration Number : 306MF10091
Registrant's Address : Calle 14, Nr. 229 (Lote 13), B1629MXA, Parque Industrial Pilar, Buenos Aires, Argenti...
Initial Date of Registration : 2024-07-03
Latest Date of Registration : 2024-07-03
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PharmaCompass offers a list of Lomustine 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 Lomustine manufacturer or Lomustine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lomustine manufacturer or Lomustine supplier.
PharmaCompass also assists you with knowing the Lomustine API Price utilized in the formulation of products. Lomustine API Price is not always fixed or binding as the Lomustine Price is obtained through a variety of data sources. The Lomustine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ICIG 1109 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ICIG 1109, including repackagers and relabelers. The FDA regulates ICIG 1109 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ICIG 1109 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 ICIG 1109 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A ICIG 1109 supplier is an individual or a company that provides ICIG 1109 active pharmaceutical ingredient (API) or ICIG 1109 finished formulations upon request. The ICIG 1109 suppliers may include ICIG 1109 API manufacturers, exporters, distributors and traders.
click here to find a list of ICIG 1109 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 ICIG 1109 Drug Master File in Japan (ICIG 1109 JDMF) empowers ICIG 1109 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 ICIG 1109 JDMF during the approval evaluation for pharmaceutical products. At the time of ICIG 1109 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 ICIG 1109 suppliers with JDMF on PharmaCompass.
