01 1Glaxo Wellcome Manufacturing Pte Ltd@[micronization process manufacturing company] Glaxo Operations UK Ltd
01 1GlaxoSmithKline Inc.
01 1vilanterol trifenatate
01 1United Kingdom
Registrant Name : GlaxoSmithKline Inc.
Registration Date : 2014-06-30
Registration Number : Su2480-12-ND
Manufacturer Name : Glaxo Wellcome Manufacturing...
Manufacturer Address : 1 Pioneer Sector 1, Singapore 628413@Priory Street, Ware, Hertfordshire, SG12 0DJ, Un...
A Vilanterol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vilanterol, including repackagers and relabelers. The FDA regulates Vilanterol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vilanterol 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 Vilanterol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Vilanterol supplier is an individual or a company that provides Vilanterol active pharmaceutical ingredient (API) or Vilanterol finished formulations upon request. The Vilanterol suppliers may include Vilanterol API manufacturers, exporters, distributors and traders.
click here to find a list of Vilanterol 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 Vilanterol Drug Master File in Korea (Vilanterol KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Vilanterol. The MFDS reviews the Vilanterol KDMF as part of the drug registration process and uses the information provided in the Vilanterol KDMF to evaluate the safety and efficacy of the drug.
After submitting a Vilanterol 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 Vilanterol API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Vilanterol suppliers with KDMF on PharmaCompass.
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