Suppliers / Mesoestetic Pharma Group, S.L

Mesoestetic Pharma Group, S.L

Spain Updated 9 July 2026

Mesoestetic Pharma Group, S.L is a finished-dose manufacturer based in Spain. It appears in 16 regulatory filings across 4 regulators, without an active US DMF or CEP on file. Its filings concentrate with DIGEMAPS (DO), EDE (AE) and EMA. Its GMP standing is certified by EMA and AEMPS (ES).

0
active US DMFs
0
valid CEPs
4
registered plants 1 with an FDA FEI number
16
filings across 4 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
EU GMP
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Barcelona, United Arab Emirates Not on file
Spain, Spain 3013582435
Barcelona, Spain Not on file
Viladecans, Spain Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DIGEMAPS (DO) 8 None
EDE (AE) 6 None
EMA 1 1
AEMPS (ES) 1 1

Questions about Mesoestetic Pharma Group, S.L

Does Mesoestetic Pharma Group, S.L hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Mesoestetic Pharma Group, S.L. It does have 16 filings with 4 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Mesoestetic Pharma Group, S.L FDA-registered?
One site operated by Mesoestetic Pharma Group, S.L carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
Where does Mesoestetic Pharma Group, S.L manufacture?
4 registered sites are on record, in United Arab Emirates and Spain (Barcelona, Spain and Viladecans among others). Every site is listed on this page with the register it came from.
Which regulators recognise Mesoestetic Pharma Group, S.L's GMP?
Current GMP certificates are on record from EMA and AEMPS (ES). 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