01 1Liquid Quimica Mexicana, S.A. De C.V.
01 1Toru Co., Ltd.
01 1precipitated calcium carbonate
01 1Mexico
precipitated calcium carbonate
Registrant Name : Toru Co., Ltd.
Registration Date : 2026-01-16
Registration Number : 20260116-211-J-2100
Manufacturer Name : Liquid Quimica Mexicana, S.A...
Manufacturer Address : Carretera Tlalnepantla-Cuautitlan Km. 31.5, Col. Loma Bonita CP 54800 Cuautitlan, Mex...
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PharmaCompass offers a list of Calcium Carbonate 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 Calcium Carbonate manufacturer or Calcium Carbonate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Calcium Carbonate manufacturer or Calcium Carbonate supplier.
A CI 77220 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CI 77220, including repackagers and relabelers. The FDA regulates CI 77220 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CI 77220 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 CI 77220 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A CI 77220 supplier is an individual or a company that provides CI 77220 active pharmaceutical ingredient (API) or CI 77220 finished formulations upon request. The CI 77220 suppliers may include CI 77220 API manufacturers, exporters, distributors and traders.
click here to find a list of CI 77220 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 CI 77220 Drug Master File in Korea (CI 77220 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of CI 77220. The MFDS reviews the CI 77220 KDMF as part of the drug registration process and uses the information provided in the CI 77220 KDMF to evaluate the safety and efficacy of the drug.
After submitting a CI 77220 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 CI 77220 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of CI 77220 suppliers with KDMF on PharmaCompass.
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