01 1Thermo Fisher Scientific Cork Limited
01 1Novartis Korea
01 1Lapatinib ditosylate
01 1U.S.A
Registrant Name : Novartis Korea
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, 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.
A Lapatinib manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lapatinib, including repackagers and relabelers. The FDA regulates Lapatinib manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lapatinib 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 Lapatinib manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Lapatinib supplier is an individual or a company that provides Lapatinib active pharmaceutical ingredient (API) or Lapatinib finished formulations upon request. The Lapatinib suppliers may include Lapatinib API manufacturers, exporters, distributors and traders.
click here to find a list of Lapatinib suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Lapatinib Drug Master File in Korea (Lapatinib KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Lapatinib. The MFDS reviews the Lapatinib KDMF as part of the drug registration process and uses the information provided in the Lapatinib KDMF to evaluate the safety and efficacy of the drug.
After submitting a Lapatinib 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 Lapatinib API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Lapatinib suppliers with KDMF on PharmaCompass.
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