Suppliers / Sopharma Ad

Sopharma Ad

Bulgaria Updated 9 July 2026

Sopharma Ad is a finished-dose manufacturer based in Bulgaria. It appears in 184 regulatory filings across 4 regulators, without an active US DMF or CEP on file. Its filings concentrate with EMA, UZPHARM (UZ) and JFDA (JO). Its GMP standing is certified by EMA.

0
active US DMFs
0
valid CEPs
1
registered plants
184
filings across 4 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
Veliko Tarnovo, Bulgaria Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA 163 1
UZPHARM (UZ) 16 None
JFDA (JO) 3 None
DAV (Vietnam) 2 None

Questions about Sopharma Ad

Does Sopharma Ad hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Sopharma Ad. It does have 184 filings with 4 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Sopharma Ad manufacture?
1 registered site is on record, in Bulgaria (Veliko Tarnovo). Every site is listed on this page with the register it came from.
Which regulators recognise Sopharma Ad'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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Sources on this page

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