01 1Corden Pharma Bergamo SPA
01 1JW Pharmaceutical Co., Ltd.
01 1Lanthanum carbonate
01 1Italy
Registrant Name : JW Pharmaceutical Co., Ltd.
Registration Date : 2005-09-08
Registration Number : Su269-3-ND
Manufacturer Name : Corden Pharma Bergamo SPA
Manufacturer Address : Via Bergamo 121, 24047 Treviglio(BG), Milano, Italy_x000D_
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A Carbonic acid, lanthanum(3+) salt (3:2) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Carbonic acid, lanthanum(3+) salt (3:2), including repackagers and relabelers. The FDA regulates Carbonic acid, lanthanum(3+) salt (3:2) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Carbonic acid, lanthanum(3+) salt (3:2) 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 Carbonic acid, lanthanum(3+) salt (3:2) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Carbonic acid, lanthanum(3+) salt (3:2) supplier is an individual or a company that provides Carbonic acid, lanthanum(3+) salt (3:2) active pharmaceutical ingredient (API) or Carbonic acid, lanthanum(3+) salt (3:2) finished formulations upon request. The Carbonic acid, lanthanum(3+) salt (3:2) suppliers may include Carbonic acid, lanthanum(3+) salt (3:2) API manufacturers, exporters, distributors and traders.
click here to find a list of Carbonic acid, lanthanum(3+) salt (3:2) suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Carbonic acid, lanthanum(3+) salt (3:2) Drug Master File in Korea (Carbonic acid, lanthanum(3+) salt (3:2) KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Carbonic acid, lanthanum(3+) salt (3:2). The MFDS reviews the Carbonic acid, lanthanum(3+) salt (3:2) KDMF as part of the drug registration process and uses the information provided in the Carbonic acid, lanthanum(3+) salt (3:2) KDMF to evaluate the safety and efficacy of the drug.
After submitting a Carbonic acid, lanthanum(3+) salt (3:2) 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 Carbonic acid, lanthanum(3+) salt (3:2) API can apply through the Korea Drug Master File (KDMF).
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