Suppliers / Medipharm Labs

Medipharm Labs

Canada 124 employees Updated 9 July 2026

Medipharm Labs is an API manufacturer based in Canada. It holds one active US drug master file. Its GMP standing is certified by ANVISA (Brazil).

1
active US DMFs
0
valid CEPs
2
registered plants 1 with an FDA FEI number
0
filings across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026.

Registered plants

Site FDA FEI
BARRIE, Canada Not on file
Canada, Canada 3015467675

What they file, and where

Molecule Regulators Docs
Cannabidiol US FDA 1

Also appears on these molecule pages

Cannabidiol API

Filings and GMP by regulator

Regulator Filings GMP certificates
ANVISA (Brazil) None 2

Questions about Medipharm Labs

Does Medipharm Labs hold a US DMF or a CEP?
Medipharm Labs holds 1 active US drug master file. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
Is Medipharm Labs FDA-registered?
One site operated by Medipharm Labs 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 Medipharm Labs manufacture?
2 registered sites are on record, in Canada (Barrie and Canada). Every site is listed on this page with the register it came from.
What does Medipharm Labs make?
1 molecule is on record against Medipharm Labs, including Cannabidiol. Each links through to that molecule's full manufacturer list.
Which regulators recognise Medipharm Labs's GMP?
Current GMP certificates are on record from ANVISA (Brazil). 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