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