01 1Dojin lyaku-Kako Co., Ltd.
01 1HanAll Biopharma Co., Ltd.
01 1Pudosteine
01 1South Korea
Registrant Name : HanAll Biopharma Co., Ltd.
Registration Date : 2004-06-22
Registration Number : 35-1-ND
Manufacturer Name : Dojin lyaku-Kako Co., Ltd.
Manufacturer Address : 263-1, Higashidai Ottozowa, Okum-machi, Futa-gun Fukishima-prefecture, Japan
37
PharmaCompass offers a list of Fudosteine 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 Fudosteine manufacturer or Fudosteine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fudosteine manufacturer or Fudosteine supplier.
PharmaCompass also assists you with knowing the Fudosteine API Price utilized in the formulation of products. Fudosteine API Price is not always fixed or binding as the Fudosteine Price is obtained through a variety of data sources. The Fudosteine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Spelear manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Spelear, including repackagers and relabelers. The FDA regulates Spelear manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Spelear API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Spelear supplier is an individual or a company that provides Spelear active pharmaceutical ingredient (API) or Spelear finished formulations upon request. The Spelear suppliers may include Spelear API manufacturers, exporters, distributors and traders.
click here to find a list of Spelear suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Spelear Drug Master File in Korea (Spelear KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Spelear. The MFDS reviews the Spelear KDMF as part of the drug registration process and uses the information provided in the Spelear KDMF to evaluate the safety and efficacy of the drug.
After submitting a Spelear 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 Spelear API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Spelear suppliers with KDMF on PharmaCompass.
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