Suppliers / Laboratorio Elea Phoenix

Laboratorio Elea Phoenix

Argentina Updated 9 July 2026

Laboratorio Elea Phoenix is a finished-dose manufacturer based in Argentina. It appears in 226 regulatory filings across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by ANVISA (Brazil) and NCELS (KZ).

0
active US DMFs
0
valid CEPs
1
registered plants
226
filings across 1 regulators

Registered plants

Site FDA FEI
BUENOS AIRES, Argentina Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
ANMAT (AR) 226 None
ANVISA (Brazil) None 1
NCELS (KZ) None 1

Questions about Laboratorio Elea Phoenix

Does Laboratorio Elea Phoenix hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Laboratorio Elea Phoenix. It does have 226 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Laboratorio Elea Phoenix manufacture?
1 registered site is on record, in Argentina (Buenos Aires). Every site is listed on this page with the register it came from.
Which regulators recognise Laboratorio Elea Phoenix's GMP?
Current GMP certificates are on record from ANVISA (Brazil) and NCELS (KZ). 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