01 1AbbVie Ireland NL BV
02 1AbbVie Operations Singapore Pte. Ltd
01 2AbbVie Korea Co., Ltd.
01 2Venetoclax
01 1Italy
02 1U.S.A
Registrant Name : AbbVie Korea Co., Ltd.
Registration Date : 2020-03-26
Registration Number : Su325-10-ND
Manufacturer Name : AbbVie Ireland NL BV
Manufacturer Address : Manorhamilton Road Sligo, Ireland
Registrant Name : AbbVie Korea Co., Ltd.
Registration Date : 2020-03-26
Registration Number : Su325-11-ND
Manufacturer Name : AbbVie Operations Singapore ...
Manufacturer Address : 23 Tuas South Avenue 6 Singapore, 637022
A Venetoclax manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Venetoclax, including repackagers and relabelers. The FDA regulates Venetoclax manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Venetoclax 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 Venetoclax manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Venetoclax supplier is an individual or a company that provides Venetoclax active pharmaceutical ingredient (API) or Venetoclax finished formulations upon request. The Venetoclax suppliers may include Venetoclax API manufacturers, exporters, distributors and traders.
click here to find a list of Venetoclax 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 Venetoclax Drug Master File in Korea (Venetoclax KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Venetoclax. The MFDS reviews the Venetoclax KDMF as part of the drug registration process and uses the information provided in the Venetoclax KDMF to evaluate the safety and efficacy of the drug.
After submitting a Venetoclax 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 Venetoclax API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Venetoclax suppliers with KDMF on PharmaCompass.
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