Suppliers / Douglas Manufacturing

Douglas Manufacturing

New Zealand Updated 9 July 2026

Douglas Manufacturing is a finished-dose manufacturer based in New Zealand. It appears in 20 regulatory filings across 4 regulators, without an active US DMF or CEP on file. Its filings concentrate with EDE (AE), NPRA (MY) and SFDA (Saudi Arabia). Its GMP standing is certified by US FDA. Its most recent recorded inspection, by US FDA, closed on 30 May 2025 as VAI.

0
active US DMFs
0
valid CEPs
2
registered plants 1 with an FDA FEI number
20
filings across 4 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
6 of 6 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 30 May 2025 VAI US FDA
  • 11 October 2019 VAI US FDA
  • 1 December 2017 VAI US FDA
  • 29 July 2016 NAI US FDA
  • 4 July 2014 VAI US FDA
  • 31 May 2011 NAI US FDA

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

Registered plants

Site FDA FEI
Auckland, United Arab Emirates Not on file
New Zealand, New Zealand 3005641565

Filings and GMP by regulator

Regulator Filings GMP certificates
EDE (AE) 12 None
NPRA (MY) 4 None
SFDA (Saudi Arabia) 3 None
MINSA (CR) 1 None
US FDA None 1

Questions about Douglas Manufacturing

Does Douglas Manufacturing hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Douglas Manufacturing. It does have 20 filings with 4 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Douglas Manufacturing FDA-registered?
One site operated by Douglas Manufacturing 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 Douglas Manufacturing's last inspection go?
The most recent inspection on record closed on 30 May 2025 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 6 inspections are on file.
Where does Douglas Manufacturing manufacture?
2 registered sites are on record, in United Arab Emirates and New Zealand (Auckland and New Zealand). Every site is listed on this page with the register it came from.
Which regulators recognise Douglas Manufacturing's GMP?
Current GMP certificates are on record from US FDA. 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 VAI, on 30 May 2025.

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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