01 1Thermo Fisher Scientific Cork Limited
01 1Novartis Korea Ltd.
01 1Lapatinib ditosylate
01 1U.S.A
Registrant Name : Novartis Korea Ltd.
Registration Date : 2007-07-24
Registration Number : 89-3-ND
Manufacturer Name : Thermo Fisher Scientific Cor...
Manufacturer Address : Currabinny, Carrigaline, Co, Cork, P43 AY66, Ireland
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PharmaCompass offers a list of Lapatinib Ditosylate 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 Lapatinib Ditosylate manufacturer or Lapatinib Ditosylate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lapatinib Ditosylate manufacturer or Lapatinib Ditosylate supplier.
PharmaCompass also assists you with knowing the Lapatinib Ditosylate API Price utilized in the formulation of products. Lapatinib Ditosylate API Price is not always fixed or binding as the Lapatinib Ditosylate Price is obtained through a variety of data sources. The Lapatinib Ditosylate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A GW282974X manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of GW282974X, including repackagers and relabelers. The FDA regulates GW282974X manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. GW282974X API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A GW282974X supplier is an individual or a company that provides GW282974X active pharmaceutical ingredient (API) or GW282974X finished formulations upon request. The GW282974X suppliers may include GW282974X API manufacturers, exporters, distributors and traders.
click here to find a list of GW282974X suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a GW282974X Drug Master File in Korea (GW282974X KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of GW282974X. The MFDS reviews the GW282974X KDMF as part of the drug registration process and uses the information provided in the GW282974X KDMF to evaluate the safety and efficacy of the drug.
After submitting a GW282974X KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their GW282974X API can apply through the Korea Drug Master File (KDMF).
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