Suppliers / Uni-Pharma Kleon Tsetis Pharmaceutical Laboratories

Uni-Pharma Kleon Tsetis Pharmaceutical Laboratories

Greece 2 duplicate records merged Updated 9 July 2026

Uni-Pharma Kleon Tsetis Pharmaceutical Laboratories is a finished-dose manufacturer based in Greece. It appears in 240 regulatory filings across 13 regulators, without an active US DMF or CEP on file. Its filings concentrate with EMA, MPA (SE) and INFARMED (PT).

0
active US DMFs
0
valid CEPs
1
registered plants
240
filings across 13 regulators

Registered plants

Site FDA FEI
Athens, United Arab Emirates Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA 146 None
MPA (SE) 29 None
INFARMED (PT) 15 None
ANSM (FR) 14 None
AEMPS (ES) 14 None
ARCSA (EC) 8 None

Questions about Uni-Pharma Kleon Tsetis Pharmaceutical Laboratories

Does Uni-Pharma Kleon Tsetis Pharmaceutical Laboratories hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Uni-Pharma Kleon Tsetis Pharmaceutical Laboratories. It does have 240 filings with 13 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Uni-Pharma Kleon Tsetis Pharmaceutical Laboratories manufacture?
1 registered site is on record, in United Arab Emirates (Athens). Every site is listed on this page with the register it came from.
Where does Uni-Pharma Kleon Tsetis Pharmaceutical Laboratories file?
Filings are on record with EMA, MPA (SE), INFARMED (PT), ANSM (FR) and 9 other regulators, 240 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