01 1BASF SE
01 1Parmarine Co., Ltd.
01 1Tocopherol acetate
01 1Germany
Registrant Name : Parmarine Co., Ltd.
Registration Date : 2024-08-09
Registration Number : 20240809-211-J-1635
Manufacturer Name : BASF SE
Manufacturer Address : Carl-Bosch-Strasse 38, 67056 Ludwigshafen, Germany
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A All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard, including repackagers and relabelers. The FDA regulates All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard 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 All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard supplier is an individual or a company that provides All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard active pharmaceutical ingredient (API) or All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard finished formulations upon request. The All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard suppliers may include All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard 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 All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard Drug Master File in Korea (All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard. The MFDS reviews the All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard KDMF as part of the drug registration process and uses the information provided in the All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard KDMF to evaluate the safety and efficacy of the drug.
After submitting a All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard 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 All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard API can apply through the Korea Drug Master File (KDMF).
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We have 1 companies offering All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard
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