01 1BIOFER SPA
01 1Sam-O Pharmaceutical Co., Ltd.
01 1Polymaltose ferric hydroxide complex
01 1Italy
Polymaltose ferric hydroxide complex
Registrant Name : Sam-O Pharmaceutical Co., Ltd.
Registration Date : 2022-01-10
Registration Number : 20220110-211-J-1113
Manufacturer Name : BIOFER SPA
Manufacturer Address : Via Canina, 2 - 41036 MEDOLLA (MO), Italy
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PharmaCompass offers a list of Iron III Hydroxide Polymaltose Complex API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Iron III Hydroxide Polymaltose Complex manufacturer or Iron III Hydroxide Polymaltose Complex supplier for your needs.
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A Iron Hydroxide Polymaltose manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Iron Hydroxide Polymaltose, including repackagers and relabelers. The FDA regulates Iron Hydroxide Polymaltose manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Iron Hydroxide Polymaltose 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 Iron Hydroxide Polymaltose supplier is an individual or a company that provides Iron Hydroxide Polymaltose active pharmaceutical ingredient (API) or Iron Hydroxide Polymaltose finished formulations upon request. The Iron Hydroxide Polymaltose suppliers may include Iron Hydroxide Polymaltose 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 Iron Hydroxide Polymaltose Drug Master File in Korea (Iron Hydroxide Polymaltose KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Iron Hydroxide Polymaltose. The MFDS reviews the Iron Hydroxide Polymaltose KDMF as part of the drug registration process and uses the information provided in the Iron Hydroxide Polymaltose KDMF to evaluate the safety and efficacy of the drug.
After submitting a Iron Hydroxide Polymaltose 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 Iron Hydroxide Polymaltose API can apply through the Korea Drug Master File (KDMF).
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