Suppliers / Laboratoire INNOTECH INTERNATIONAL

Laboratoire INNOTECH INTERNATIONAL

France 28 employees 2 duplicate records merged Updated 9 July 2026

Laboratoire INNOTECH INTERNATIONAL is a finished-dose manufacturer based in France. It appears in 111 regulatory filings across 14 regulators, without an active US DMF or CEP on file. Its filings concentrate with RAMA (GE), EMA and RCETH (BY). Its GMP standing is certified by TMDA (TZ).

0
active US DMFs
0
valid CEPs
0
registered plants
111
filings across 14 regulators

Filings and GMP by regulator

Regulator Filings GMP certificates
RAMA (GE) 22 None
EMA 19 None
RCETH (BY) 18 None
ANSM (FR) 17 None
DPM (TN) 9 None
ANPP (DZ) 7 None
TMDA (TZ) None 1

Limited public record

Beyond the filing counts above, the public registers hold no plant, inspection or portfolio detail for this company as at 9 July 2026. We report that as a gap rather than inferring an answer.

Questions about Laboratoire INNOTECH INTERNATIONAL

Does Laboratoire INNOTECH INTERNATIONAL hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Laboratoire INNOTECH INTERNATIONAL. It does have 111 filings with 14 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Which regulators recognise Laboratoire INNOTECH INTERNATIONAL's GMP?
Current GMP certificates are on record from TMDA (TZ). 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