01 1Azico Biophore India Private Limited
01 1Aging Life Science Co., Ltd.
01 1Liothironin sodium
01 1India
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2020-11-25
Registration Number : 20201125-211-J-790
Manufacturer Name : Azico Biophore India Private...
Manufacturer Address : Plot Number 40/A, Sy. No. 13,15,16,51,52 & 182, JN.Pharma city, Thanam(V), Anakapalli...
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PharmaCompass offers a list of Liothyronine Sodium 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 Liothyronine Sodium manufacturer or Liothyronine Sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Liothyronine Sodium manufacturer or Liothyronine Sodium supplier.
A Liothyronine Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Liothyronine Sodium, including repackagers and relabelers. The FDA regulates Liothyronine Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Liothyronine Sodium 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 Liothyronine Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Liothyronine Sodium supplier is an individual or a company that provides Liothyronine Sodium active pharmaceutical ingredient (API) or Liothyronine Sodium finished formulations upon request. The Liothyronine Sodium suppliers may include Liothyronine Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Liothyronine Sodium 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 Liothyronine Sodium Drug Master File in Korea (Liothyronine Sodium KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Liothyronine Sodium. The MFDS reviews the Liothyronine Sodium KDMF as part of the drug registration process and uses the information provided in the Liothyronine Sodium KDMF to evaluate the safety and efficacy of the drug.
After submitting a Liothyronine Sodium 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 Liothyronine Sodium API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Liothyronine Sodium suppliers with KDMF on PharmaCompass.
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