01 1Sterling Wisconsin LLC
01 1Handok Co., Ltd.
01 1Avatrombopag Maleate
01 1United Kingdom
Registrant Name : Handok Co., Ltd.
Registration Date : 2024-11-26
Registration Number : Su318-7-ND
Manufacturer Name : Sterling Wisconsin LLC
Manufacturer Address : W130 N10497 Washington Drive Germantown, WI, 53022, USA
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PharmaCompass offers a list of Avatrombopag Maleate 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 Avatrombopag Maleate manufacturer or Avatrombopag Maleate supplier for your needs.
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PharmaCompass also assists you with knowing the Avatrombopag Maleate API Price utilized in the formulation of products. Avatrombopag Maleate API Price is not always fixed or binding as the Avatrombopag Maleate Price is obtained through a variety of data sources. The Avatrombopag Maleate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Doptelet (TN) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Doptelet (TN), including repackagers and relabelers. The FDA regulates Doptelet (TN) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Doptelet (TN) 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 Doptelet (TN) supplier is an individual or a company that provides Doptelet (TN) active pharmaceutical ingredient (API) or Doptelet (TN) finished formulations upon request. The Doptelet (TN) suppliers may include Doptelet (TN) API manufacturers, exporters, distributors and traders.
click here to find a list of Doptelet (TN) 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 Doptelet (TN) Drug Master File in Korea (Doptelet (TN) KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Doptelet (TN). The MFDS reviews the Doptelet (TN) KDMF as part of the drug registration process and uses the information provided in the Doptelet (TN) KDMF to evaluate the safety and efficacy of the drug.
After submitting a Doptelet (TN) 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 Doptelet (TN) API can apply through the Korea Drug Master File (KDMF).
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