01 1Siegfried PharmaChemikalien Minden GmbH
01 1CTC Bio Co., Ltd.
01 1Caffeine Anhydrous
01 1Switzerland
Registrant Name : CTC Bio Co., Ltd.
Registration Date : 2022-08-08
Registration Number : 20220808-211-J-1341
Manufacturer Name : Siegfried PharmaChemikalien ...
Manufacturer Address : Karlstraße 15-39, 42-44 32423 Minden, Germany
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PharmaCompass offers a list of Caffeine 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 Caffeine manufacturer or Caffeine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Caffeine manufacturer or Caffeine supplier.
PharmaCompass also assists you with knowing the Caffeine API Price utilized in the formulation of products. Caffeine API Price is not always fixed or binding as the Caffeine Price is obtained through a variety of data sources. The Caffeine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CFF manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CFF, including repackagers and relabelers. The FDA regulates CFF manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CFF 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 CFF manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CFF supplier is an individual or a company that provides CFF active pharmaceutical ingredient (API) or CFF finished formulations upon request. The CFF suppliers may include CFF API manufacturers, exporters, distributors and traders.
click here to find a list of CFF suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price 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 CFF Drug Master File in Korea (CFF KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of CFF. The MFDS reviews the CFF KDMF as part of the drug registration process and uses the information provided in the CFF KDMF to evaluate the safety and efficacy of the drug.
After submitting a CFF 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 CFF API can apply through the Korea Drug Master File (KDMF).
click here to find a list of CFF suppliers with KDMF on PharmaCompass.
