Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
01 1Centrient Pharmaceuticals (Zibo) Co., Ltd.
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Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2017-04-11
Registration Number : 20170411-20-A-326-20
Manufacturer Name : Centrient Pharmaceuticals (Z...
Manufacturer Address : West of Baoshan Road, North of Beiling Road, High-Tech Zone, Zibo Shandong Province, ...
A Cefaclor manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefaclor, including repackagers and relabelers. The FDA regulates Cefaclor manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefaclor API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Cefaclor manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cefaclor supplier is an individual or a company that provides Cefaclor active pharmaceutical ingredient (API) or Cefaclor finished formulations upon request. The Cefaclor suppliers may include Cefaclor API manufacturers, exporters, distributors and traders.
click here to find a list of Cefaclor 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 Cefaclor Drug Master File in Korea (Cefaclor KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Cefaclor. The MFDS reviews the Cefaclor KDMF as part of the drug registration process and uses the information provided in the Cefaclor KDMF to evaluate the safety and efficacy of the drug.
After submitting a Cefaclor 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 Cefaclor API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Cefaclor suppliers with KDMF on PharmaCompass.
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