01 1MSN Laboratories Private Limited
01 1Kukjeon Pharmaceutical Co., Ltd.
01 1Crizotinib
01 1India
Registrant Name : Kukjeon Pharmaceutical Co., Ltd.
Registration Date : 2025-02-12
Registration Number : Su173-53-ND
Manufacturer Name : MSN Laboratories Private Lim...
Manufacturer Address : Unit-III, Sy. No. 111/E & 111/EE, Cheriyal (Village), Kandi (Mandal), Sangareddy Dist...
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PharmaCompass offers a list of Crizotinib 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 Crizotinib manufacturer or Crizotinib supplier for your needs.
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PharmaCompass also assists you with knowing the Crizotinib API Price utilized in the formulation of products. Crizotinib API Price is not always fixed or binding as the Crizotinib Price is obtained through a variety of data sources. The Crizotinib Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A SB431542, SB 431542 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of SB431542, SB 431542, including repackagers and relabelers. The FDA regulates SB431542, SB 431542 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. SB431542, SB 431542 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 SB431542, SB 431542 supplier is an individual or a company that provides SB431542, SB 431542 active pharmaceutical ingredient (API) or SB431542, SB 431542 finished formulations upon request. The SB431542, SB 431542 suppliers may include SB431542, SB 431542 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 SB431542, SB 431542 Drug Master File in Korea (SB431542, SB 431542 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of SB431542, SB 431542. The MFDS reviews the SB431542, SB 431542 KDMF as part of the drug registration process and uses the information provided in the SB431542, SB 431542 KDMF to evaluate the safety and efficacy of the drug.
After submitting a SB431542, SB 431542 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 SB431542, SB 431542 API can apply through the Korea Drug Master File (KDMF).
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