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01 1Hanmi Precision Chemical Co., Ltd.
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01 1Hanmi Precision Chemical Co., Ltd.
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01 1Olmutinib hydrochloride monohydrate
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01 1South Korea
Olmutinib hydrochloride monohydrate
Registrant Name : Hanmi Precision Chemical Co., Ltd.
Registration Date : 2016-04-22
Registration Number : 1444-4-ND
Manufacturer Name : Hanmi Precision Chemical Co....
Manufacturer Address : 57 Gyeongje-ro, Siheung-si, Gyeonggi-do
50
PharmaCompass offers a list of Olmutinib 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 Olmutinib manufacturer or Olmutinib supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Olmutinib manufacturer or Olmutinib supplier.
PharmaCompass also assists you with knowing the Olmutinib API Price utilized in the formulation of products. Olmutinib API Price is not always fixed or binding as the Olmutinib Price is obtained through a variety of data sources. The Olmutinib Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A olita manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of olita, including repackagers and relabelers. The FDA regulates olita manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. olita API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A olita supplier is an individual or a company that provides olita active pharmaceutical ingredient (API) or olita finished formulations upon request. The olita suppliers may include olita API manufacturers, exporters, distributors and traders.
click here to find a list of olita 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 olita Drug Master File in Korea (olita KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of olita. The MFDS reviews the olita KDMF as part of the drug registration process and uses the information provided in the olita KDMF to evaluate the safety and efficacy of the drug.
After submitting a olita 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 olita API can apply through the Korea Drug Master File (KDMF).
click here to find a list of olita suppliers with KDMF on PharmaCompass.
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