Suppliers / Pharmidea

Pharmidea

Latvia Updated 9 July 2026

Pharmidea is a contract manufacturer based in Latvia. It appears in 18 regulatory filings across 7 regulators, without an active US DMF or CEP on file. Its filings concentrate with EMA, ARCSA (EC) and EDE (AE).

0
active US DMFs
0
valid CEPs
2
registered plants
18
filings across 7 regulators

Registered plants

Site FDA FEI
Olaine, United Arab Emirates Not on file
OLAINE, Latvia Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA 5 None
ARCSA (EC) 4 None
EDE (AE) 3 None
INFARMED (PT) 2 None
MINSA (CR) 2 None
NPRA (MY) 1 None

Questions about Pharmidea

Does Pharmidea hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Pharmidea. It does have 18 filings with 7 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Pharmidea manufacture?
2 registered sites are on record, in United Arab Emirates and Latvia (Olaine and Olaine). Every site is listed on this page with the register it came from.
Where does Pharmidea file?
Filings are on record with EMA, ARCSA (EC), EDE (AE), INFARMED (PT) and 3 other regulators, 18 in total.

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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Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability