Suppliers / Remedica

Remedica

Cyprus 423 employees 3 duplicate records merged Updated 9 July 2026

Remedica is a finished-dose manufacturer based in Cyprus. It appears in 441 regulatory filings across 16 regulators, without an active US DMF or CEP on file. Its filings concentrate with EMA, TMDA (TZ) and EFDA (ET). Its GMP standing is certified by MFDS (Korea), ANVISA (Brazil) and GOSPHARMNADZOR (BY), among 5 authorities.

0
active US DMFs
0
valid CEPs
2
registered plants
441
filings across 16 regulators

Registered plants

Site FDA FEI
Limassol, United Arab Emirates Not on file
LIMASSOL, Cyprus Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA 174 None
TMDA (TZ) 71 1
EFDA (ET) 44 None
MCAZ (ZW) 35 None
EDE (AE) 33 None
JFDA (JO) 22 None
MFDS (Korea) None 2
ANVISA (Brazil) None 1
GOSPHARMNADZOR (BY) None 1
NAFDAC (NG) None 1

Questions about Remedica

Does Remedica hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Remedica. It does have 441 filings with 16 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Remedica manufacture?
2 registered sites are on record, in United Arab Emirates and Cyprus (Limassol and Limassol). Every site is listed on this page with the register it came from.
Which regulators recognise Remedica's GMP?
Current GMP certificates are on record from MFDS (Korea), ANVISA (Brazil), GOSPHARMNADZOR (BY), TMDA (TZ) and NAFDAC (NG). 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