Minakem delivers API, HPAPI, steroids & CDMO services for generics with FDA/GMP certification, regulatory know-how & proven success.
01 1Minakem High Potent SA
02 1Ajinomoto Omnichem NV
03 1AstraZeneca UK Ltd.
04 1INDUSTRIAL CHIMICA SRL
05 1Industriale Chimica Srl
06 1ScinoPharm Taiwan, Ltd.
07 1Sinopep-Allsino Biopharmaceutical Co.,LTD
Minakem delivers API, HPAPI, steroids & CDMO services for generics with FDA/GMP certification, regulatory know-how & proven success.
Registrant Name : AstraZeneca Korea Ltd.
Registration Date : 2014-10-24
Registration Number : Su3042-8-ND
Manufacturer Name : Minakem High Potent SA
Manufacturer Address : Rue Fonds Jean Paques, 8, Mont-Saint-Guibert, 1435, Belgium
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PharmaCompass offers a list of Fulvestrant 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 Fulvestrant manufacturer or Fulvestrant supplier for your needs.
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A Tox21_202604 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_202604, including repackagers and relabelers. The FDA regulates Tox21_202604 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_202604 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_202604 supplier is an individual or a company that provides Tox21_202604 active pharmaceutical ingredient (API) or Tox21_202604 finished formulations upon request. The Tox21_202604 suppliers may include Tox21_202604 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_202604 Drug Master File in Korea (Tox21_202604 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Tox21_202604. The MFDS reviews the Tox21_202604 KDMF as part of the drug registration process and uses the information provided in the Tox21_202604 KDMF to evaluate the safety and efficacy of the drug.
After submitting a Tox21_202604 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_202604 API can apply through the Korea Drug Master File (KDMF).
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We have 6 companies offering Tox21_202604
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