01 1Bayer AG
01 1Bayer Korea Ltd.
01 1IOB-DTPA
01 1Germany
Registrant Name : Bayer Korea Ltd.
Registration Date : 2006-05-11
Registration Number : 309-3-ND
Manufacturer Name : Bayer AG
Manufacturer Address : Ernst-Schering-Straße 14 59192 Bergkamen, Germany
90
PharmaCompass offers a list of Pentetic Acid 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 Pentetic Acid manufacturer or Pentetic Acid supplier for your needs.
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A Glycine, N,N-bis(2-(bis(carboxymethyl)amino)ethyl)- manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glycine, N,N-bis(2-(bis(carboxymethyl)amino)ethyl)-, including repackagers and relabelers. The FDA regulates Glycine, N,N-bis(2-(bis(carboxymethyl)amino)ethyl)- manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glycine, N,N-bis(2-(bis(carboxymethyl)amino)ethyl)- 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 Glycine, N,N-bis(2-(bis(carboxymethyl)amino)ethyl)- supplier is an individual or a company that provides Glycine, N,N-bis(2-(bis(carboxymethyl)amino)ethyl)- active pharmaceutical ingredient (API) or Glycine, N,N-bis(2-(bis(carboxymethyl)amino)ethyl)- finished formulations upon request. The Glycine, N,N-bis(2-(bis(carboxymethyl)amino)ethyl)- suppliers may include Glycine, N,N-bis(2-(bis(carboxymethyl)amino)ethyl)- 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 Glycine, N,N-bis(2-(bis(carboxymethyl)amino)ethyl)- Drug Master File in Korea (Glycine, N,N-bis(2-(bis(carboxymethyl)amino)ethyl)- KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Glycine, N,N-bis(2-(bis(carboxymethyl)amino)ethyl)-. The MFDS reviews the Glycine, N,N-bis(2-(bis(carboxymethyl)amino)ethyl)- KDMF as part of the drug registration process and uses the information provided in the Glycine, N,N-bis(2-(bis(carboxymethyl)amino)ethyl)- KDMF to evaluate the safety and efficacy of the drug.
After submitting a Glycine, N,N-bis(2-(bis(carboxymethyl)amino)ethyl)- 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 Glycine, N,N-bis(2-(bis(carboxymethyl)amino)ethyl)- API can apply through the Korea Drug Master File (KDMF).
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