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 Trifenatate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vilanterol Trifenatate, including repackagers and relabelers. The FDA regulates Vilanterol Trifenatate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vilanterol Trifenatate 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 Trifenatate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Vilanterol Trifenatate supplier is an individual or a company that provides Vilanterol Trifenatate active pharmaceutical ingredient (API) or Vilanterol Trifenatate finished formulations upon request. The Vilanterol Trifenatate suppliers may include Vilanterol Trifenatate API manufacturers, exporters, distributors and traders.
click here to find a list of Vilanterol Trifenatate 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 Trifenatate Drug Master File in Korea (Vilanterol Trifenatate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Vilanterol Trifenatate. The MFDS reviews the Vilanterol Trifenatate KDMF as part of the drug registration process and uses the information provided in the Vilanterol Trifenatate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Vilanterol Trifenatate 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 Trifenatate API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Vilanterol Trifenatate suppliers with KDMF on PharmaCompass.
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