Suppliers / Aqvida

Aqvida

Germany 72 employees Updated 9 July 2026

Aqvida is a finished-dose manufacturer based in Germany. It appears in 68 regulatory filings across 10 regulators, without an active US DMF or CEP on file. Its filings concentrate with EMA, EDE (AE) and DPM (TN). Its GMP standing is certified by ZLG (DE) and EMA. Its most recent recorded inspection, by US FDA, closed on 8 December 2022 as VAI.

0
active US DMFs
0
valid CEPs
5
registered plants 1 with an FDA FEI number
68
filings across 10 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
1 of 1 confirmed
EU GMP
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026. EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Inspection history

  • 8 December 2022 VAI US FDA

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

Registered plants

Site FDA FEI
Hamburg, United Arab Emirates Not on file
Dassow, United Arab Emirates Not on file
DASSOW, Germany Not on file
Germany, Germany 3017440477
Hamburg, Germany Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA 16 2
EDE (AE) 12 None
DPM (TN) 9 None
ARCSA (EC) 9 None
SFDA (Saudi Arabia) 6 None
EFDA (ET) 5 None
ZLG (DE) None 10

Questions about Aqvida

Does Aqvida hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Aqvida. It does have 68 filings with 10 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Aqvida FDA-registered?
One site operated by Aqvida 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 Aqvida's last inspection go?
The most recent inspection on record closed on 8 December 2022 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 1 inspection is on file.
Where does Aqvida manufacture?
5 registered sites are on record, in United Arab Emirates and Germany (Hamburg, Dassow and Dassow among others). Every site is listed on this page with the register it came from.
Which regulators recognise Aqvida's GMP?
Current GMP certificates are on record from ZLG (DE) and EMA. 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 8 December 2022.

Comparable suppliers

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Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

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