01 1BIOFER SPA
01 1Samoh Pharmaceutical Co., Ltd.
01 1Polymaltose ferric hydroxide complex salt
01 1Italy
Polymaltose ferric hydroxide complex salt
Registrant Name : Samoh 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
46
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PharmaCompass also assists you with knowing the Iron III Hydroxide Polymaltose Complex API Price utilized in the formulation of products. Iron III Hydroxide Polymaltose Complex API Price is not always fixed or binding as the Iron III Hydroxide Polymaltose Complex Price is obtained through a variety of data sources. The Iron III Hydroxide Polymaltose Complex Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A teferrol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of teferrol, including repackagers and relabelers. The FDA regulates teferrol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. teferrol 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 teferrol supplier is an individual or a company that provides teferrol active pharmaceutical ingredient (API) or teferrol finished formulations upon request. The teferrol suppliers may include teferrol 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 teferrol Drug Master File in Korea (teferrol KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of teferrol. The MFDS reviews the teferrol KDMF as part of the drug registration process and uses the information provided in the teferrol KDMF to evaluate the safety and efficacy of the drug.
After submitting a teferrol 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 teferrol API can apply through the Korea Drug Master File (KDMF).
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