01 1Gnosis Bioreseach SA
01 1Sam-O Pharmaceutical Co., Ltd.
01 1S-adenosyl-L-methionine sulfate tosylate
01 1France
S-adenosyl-L-methionine sulfate tosylate
Registrant Name : Sam-O Pharmaceutical Co., Ltd.
Registration Date : 2018-12-04
Registration Number : 20181204-209-J-143
Manufacturer Name : Gnosis Bioreseach SA
Manufacturer Address : Via Lischedi, 6592 Sant'Antonino Switzerland
76
PharmaCompass offers a list of Ademetionine Disulfate Tosylate 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 Ademetionine Disulfate Tosylate manufacturer or Ademetionine Disulfate Tosylate supplier for your needs.
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A Ademetionine Disulfate Tosylate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ademetionine Disulfate Tosylate, including repackagers and relabelers. The FDA regulates Ademetionine Disulfate Tosylate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ademetionine Disulfate Tosylate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Ademetionine Disulfate Tosylate supplier is an individual or a company that provides Ademetionine Disulfate Tosylate active pharmaceutical ingredient (API) or Ademetionine Disulfate Tosylate finished formulations upon request. The Ademetionine Disulfate Tosylate suppliers may include Ademetionine Disulfate Tosylate API manufacturers, exporters, distributors and traders.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Ademetionine Disulfate Tosylate Drug Master File in Korea (Ademetionine Disulfate Tosylate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Ademetionine Disulfate Tosylate. The MFDS reviews the Ademetionine Disulfate Tosylate KDMF as part of the drug registration process and uses the information provided in the Ademetionine Disulfate Tosylate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Ademetionine Disulfate Tosylate 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 Ademetionine Disulfate Tosylate API can apply through the Korea Drug Master File (KDMF).
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