01 1Glaxo Wellcome Manufacturing Pte Ltd@[micronization process manufacturing company] Glaxo Operations UK Ltd
01 1GlaxoSmithKline Inc.
01 1Eumeclidinium bromide
01 1United Kingdom
Registrant Name : GlaxoSmithKline Inc.
Registration Date : 2014-07-01
Registration Number : Su2480-13-ND
Manufacturer Name : Glaxo Wellcome Manufacturing...
Manufacturer Address : 1 Pioneer Sector 1, Singapore 628413@Priory Street, Ware, Hertfordshire, SG12 0DJ, Un...
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PharmaCompass offers a list of Umeclidinium Bromide 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 Umeclidinium Bromide manufacturer or Umeclidinium Bromide supplier for your needs.
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A Umeclidinium Bromide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Umeclidinium Bromide, including repackagers and relabelers. The FDA regulates Umeclidinium Bromide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Umeclidinium Bromide 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 Umeclidinium Bromide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Umeclidinium Bromide supplier is an individual or a company that provides Umeclidinium Bromide active pharmaceutical ingredient (API) or Umeclidinium Bromide finished formulations upon request. The Umeclidinium Bromide suppliers may include Umeclidinium Bromide API manufacturers, exporters, distributors and traders.
click here to find a list of Umeclidinium Bromide 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 Umeclidinium Bromide Drug Master File in Korea (Umeclidinium Bromide KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Umeclidinium Bromide. The MFDS reviews the Umeclidinium Bromide KDMF as part of the drug registration process and uses the information provided in the Umeclidinium Bromide KDMF to evaluate the safety and efficacy of the drug.
After submitting a Umeclidinium Bromide 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 Umeclidinium Bromide API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Umeclidinium Bromide suppliers with KDMF on PharmaCompass.
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