01 1Glaxo Wellcome Manufacturing Pte Ltd@[micronization process manufacturing company] Glaxo Operations UK Ltd
01 1GlaxoSmithKline Inc.
01 1Umeclidinium bromide
01 1United Kingdom
Registrant Name : GlaxoSmithKline Inc.
Registration Date : 2014-07-01
Registration Number : Number 2480-13-ND
Manufacturer Name : Glaxo Wellcome Manufacturing...
Manufacturer Address : 1 Pioneer Sector 1, Singapore 628413@Priory Street, Ware, Hertfordshire, SG12 0DJ, Un...
17
PharmaCompass offers a list of Umeclidinium Bromide 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 Umeclidinium Bromide manufacturer or Umeclidinium Bromide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Umeclidinium Bromide manufacturer or Umeclidinium Bromide supplier.
PharmaCompass also assists you with knowing the Umeclidinium Bromide API Price utilized in the formulation of products. Umeclidinium Bromide API Price is not always fixed or binding as the Umeclidinium Bromide Price is obtained through a variety of data sources. The Umeclidinium Bromide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 869113-09-7 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 869113-09-7, including repackagers and relabelers. The FDA regulates 869113-09-7 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 869113-09-7 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 869113-09-7 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 869113-09-7 supplier is an individual or a company that provides 869113-09-7 active pharmaceutical ingredient (API) or 869113-09-7 finished formulations upon request. The 869113-09-7 suppliers may include 869113-09-7 API manufacturers, exporters, distributors and traders.
click here to find a list of 869113-09-7 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 869113-09-7 Drug Master File in Korea (869113-09-7 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of 869113-09-7. The MFDS reviews the 869113-09-7 KDMF as part of the drug registration process and uses the information provided in the 869113-09-7 KDMF to evaluate the safety and efficacy of the drug.
After submitting a 869113-09-7 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 869113-09-7 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of 869113-09-7 suppliers with KDMF on PharmaCompass.
