Suppliers / "PRO.MED.CS Praha

"PRO.MED.CS Praha

Czech Republic Updated 9 July 2026

"PRO.MED.CS Praha is a finished-dose manufacturer based in Czech Republic. It appears in 196 regulatory filings across 13 regulators, without an active US DMF or CEP on file. Its filings concentrate with EMA, RAMA (GE) and AIFA (IT). Its GMP standing is certified by EMA and UZPHARM (UZ).

0
active US DMFs
0
valid CEPs
3
registered plants
196
filings across 13 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
Prauge, United Arab Emirates Not on file
Praha 4, Czech Republic Not on file
Hostivice, Czech Republic Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA 122 16
RAMA (GE) 17 None
AIFA (IT) 14 None
URPL (PL) 11 None
MPA (SE) 7 None
RCETH (BY) 7 None
UZPHARM (UZ) None 1

Questions about "PRO.MED.CS Praha

Does "PRO.MED.CS Praha hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for "PRO.MED.CS Praha. It does have 196 filings with 13 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does "PRO.MED.CS Praha manufacture?
3 registered sites are on record, in United Arab Emirates and Czech Republic (Prauge, Praha 4 and Hostivice). Every site is listed on this page with the register it came from.
Which regulators recognise "PRO.MED.CS Praha's GMP?
Current GMP certificates are on record from EMA and UZPHARM (UZ). 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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Sources on this page

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