01 2Chemische Fabrik Berg GmbH@Benechim SPRL
02 1Chemische Fabrik Berg GmbH@Benechim SRL
03 1Excella GmbH & Co. KG
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2020-08-05
Registration Number : 20200623-209-J-492(2)
Manufacturer Name : Chemische Fabrik Berg GmbH@B...
Manufacturer Address : Mainthalstraβe 3, 06749 Bitterfeld-Wolfen, Germany@Rue Rene Magritte 163 Lessines 78...
Registrant Name : Korea United Pharmaceutical Co., Ltd.
Registration Date : 2020-07-30
Registration Number : 20200623-209-J-492(1)
Manufacturer Name : Chemische Fabrik Berg GmbH@B...
Manufacturer Address : Mainthalstraβe 3, 06749 Bitterfeld-Wolfen, Germany@Rue Rene Magritte 163 Lessines 78...
Registrant Name : Kwangdong Pharmaceutical Co., Ltd.
Registration Date : 2020-06-23
Registration Number : 20200623-209-J-492
Manufacturer Name : Chemische Fabrik Berg GmbH@B...
Manufacturer Address : Mainthalstraβe 3, 06749 Bitterfeld-Wolfen, Germany@Rue Rene Magritte 163 Lessines 78...
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A Tox21_300274 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_300274, including repackagers and relabelers. The FDA regulates Tox21_300274 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_300274 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 Tox21_300274 supplier is an individual or a company that provides Tox21_300274 active pharmaceutical ingredient (API) or Tox21_300274 finished formulations upon request. The Tox21_300274 suppliers may include Tox21_300274 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 Tox21_300274 Drug Master File in Korea (Tox21_300274 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Tox21_300274. The MFDS reviews the Tox21_300274 KDMF as part of the drug registration process and uses the information provided in the Tox21_300274 KDMF to evaluate the safety and efficacy of the drug.
After submitting a Tox21_300274 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 Tox21_300274 API can apply through the Korea Drug Master File (KDMF).
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