Suppliers / Alcon Research

Alcon Research

United States 4 duplicate records merged Updated 9 July 2026

Alcon Research is a finished-dose manufacturer based in United States. It appears in 79 regulatory filings across 6 regulators, without an active US DMF or CEP on file. Its filings concentrate with EDE (AE), ARCSA (EC) and INVIMA (CO). Its GMP standing is certified by ANVISA (Brazil) and MFDS (Korea). Its most recent recorded inspection, by US FDA, closed on 15 September 2022 as NAI.

0
active US DMFs
0
valid CEPs
5
registered plants 1 with an FDA FEI number
79
filings across 6 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
8 of 8 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 15 September 2022 NAI US FDA
  • 24 September 2018 NAI US FDA
  • 4 August 2017 VAI US FDA
  • 23 May 2016 NAI US FDA
  • 1 May 2015 NAI US FDA
  • 8 May 2013 VAI US FDA
  • 29 March 2012 VAI US FDA
  • 21 October 2010 VAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
Huntington, United Arab Emirates Not on file
Fort Worth, United Arab Emirates Not on file
Fort Worth, United Arab Emirates Not on file
FORT WORTH, United States Not on file
Fort Worth, United States 1610287

Filings and GMP by regulator

Regulator Filings GMP certificates
EDE (AE) 24 None
ARCSA (EC) 23 None
INVIMA (CO) 12 None
MINSA (CR) 8 None
DIGEMAPS (DO) 7 None
NPRA (MY) 5 None
ANVISA (Brazil) None 2
MFDS (Korea) None 2

Questions about Alcon Research

Does Alcon Research hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Alcon Research. It does have 79 filings with 6 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Alcon Research FDA-registered?
One site operated by Alcon Research carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did Alcon Research's last inspection go?
The most recent inspection on record closed on 15 September 2022 as NAI (No Action Indicated: nothing objectionable was found). 8 inspections are on file.
Where does Alcon Research manufacture?
5 registered sites are on record, in United Arab Emirates and United States (Huntington, Fort Worth and Fort Worth among others). Every site is listed on this page with the register it came from.
Which regulators recognise Alcon Research's GMP?
Current GMP certificates are on record from ANVISA (Brazil) and MFDS (Korea). GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

Answered from this company's own record. Where a register holds nothing, the question is not asked rather than answered with a zero. How we count our figures.

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Open risk flags

  • The most recent inspection outcome was NAI, on 15 September 2022.

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Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates