01 1Gnosis Bioresearch SA
01 1Abbott Korea Ltd.
01 1Ademethionine 1,4-butanedisulfonate
01 1France
Ademethionine 1,4-butanedisulfonate
Registrant Name : Abbott Korea Ltd.
Registration Date : 2020-08-25
Registration Number : 20200825-209-J-722
Manufacturer Name : Gnosis Bioresearch SA
Manufacturer Address : Via Lischedi, 6592 Sant't Antonino Switzerland
79
PharmaCompass offers a list of Ademetionine 1,4-Butanedisulfonate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Ademetionine 1,4-Butanedisulfonate manufacturer or Ademetionine 1,4-Butanedisulfonate supplier for your needs.
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PharmaCompass also assists you with knowing the Ademetionine 1,4-Butanedisulfonate API Price utilized in the formulation of products. Ademetionine 1,4-Butanedisulfonate API Price is not always fixed or binding as the Ademetionine 1,4-Butanedisulfonate Price is obtained through a variety of data sources. The Ademetionine 1,4-Butanedisulfonate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A SAMe-1,4-Butanedisulfonate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of SAMe-1,4-Butanedisulfonate, including repackagers and relabelers. The FDA regulates SAMe-1,4-Butanedisulfonate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. SAMe-1,4-Butanedisulfonate 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 SAMe-1,4-Butanedisulfonate supplier is an individual or a company that provides SAMe-1,4-Butanedisulfonate active pharmaceutical ingredient (API) or SAMe-1,4-Butanedisulfonate finished formulations upon request. The SAMe-1,4-Butanedisulfonate suppliers may include SAMe-1,4-Butanedisulfonate 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 SAMe-1,4-Butanedisulfonate Drug Master File in Korea (SAMe-1,4-Butanedisulfonate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of SAMe-1,4-Butanedisulfonate. The MFDS reviews the SAMe-1,4-Butanedisulfonate KDMF as part of the drug registration process and uses the information provided in the SAMe-1,4-Butanedisulfonate KDMF to evaluate the safety and efficacy of the drug.
After submitting a SAMe-1,4-Butanedisulfonate 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 SAMe-1,4-Butanedisulfonate API can apply through the Korea Drug Master File (KDMF).
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