01 1Aptuit(UK) Ltd
01 1SK Chemicals Co., Ltd.
01 1Provatriptan
01 1Germany
Registrant Name : SK Chemicals Co., Ltd.
Registration Date : 2008-05-07
Registration Number : Su4827-2-ND
Manufacturer Name : Aptuit(UK) Ltd
Manufacturer Address : 150 Brook Drive, Milton Park, Abingdon, Oxfordshire, OX14 4SD, UK_x000D_
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PharmaCompass offers a list of Frovatriptan 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 Frovatriptan manufacturer or Frovatriptan supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Frovatriptan manufacturer or Frovatriptan supplier.
A Frovatriptan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Frovatriptan, including repackagers and relabelers. The FDA regulates Frovatriptan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Frovatriptan 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 Frovatriptan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Frovatriptan supplier is an individual or a company that provides Frovatriptan active pharmaceutical ingredient (API) or Frovatriptan finished formulations upon request. The Frovatriptan suppliers may include Frovatriptan API manufacturers, exporters, distributors and traders.
click here to find a list of Frovatriptan 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 Frovatriptan Drug Master File in Korea (Frovatriptan KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Frovatriptan. The MFDS reviews the Frovatriptan KDMF as part of the drug registration process and uses the information provided in the Frovatriptan KDMF to evaluate the safety and efficacy of the drug.
After submitting a Frovatriptan 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 Frovatriptan API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Frovatriptan suppliers with KDMF on PharmaCompass.
