Suppliers / Pinewood Laboratories

Pinewood Laboratories

Ireland Updated 9 July 2026

Pinewood Laboratories is a finished-dose manufacturer based in Ireland. It appears in 160 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with EMA and MPA (SE). Its GMP standing is certified by EMA.

0
active US DMFs
0
valid CEPs
2
registered plants
160
filings across 2 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
1 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Dublin 12, Ireland Not on file
Co Tipperary, Ireland Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA 156 3
MPA (SE) 4 None

Questions about Pinewood Laboratories

Does Pinewood Laboratories hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Pinewood Laboratories. It does have 160 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Pinewood Laboratories manufacture?
2 registered sites are on record, in Ireland (Dublin 12 and Co Tipperary). Every site is listed on this page with the register it came from.
Which regulators recognise Pinewood Laboratories's GMP?
Current GMP certificates are on record from 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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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