Suppliers / Pharmascience

Pharmascience

Canada Updated 9 July 2026

Pharmascience is a finished-dose manufacturer based in Canada. It appears in 1,883 regulatory filings across 13 regulators, without an active US DMF or CEP on file. Its filings concentrate with Health Canada, ANVISA (Brazil) and DAV (Vietnam). Its GMP standing is certified by ANVISA (Brazil), MFDS (Korea) and EMA, among 4 authorities. Its most recent recorded inspection, by US FDA, closed on 13 February 2024 as VAI.

0
active US DMFs
0
valid CEPs
4
registered plants 1 with an FDA FEI number
1,883
filings across 13 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
5 of 5 confirmed
EU GMP
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026. EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Inspection history

  • 13 February 2024 VAI US FDA
  • 18 June 2019 VAI US FDA
  • 5 February 2018 NAI US FDA
  • 17 November 2014 NAI US FDA
  • 13 July 2010 NAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
Montreal, United Arab Emirates Not on file
BETIM, Brazil Not on file
Canada, Canada 3002806578
Nicosia, Cyprus Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
Health Canada 1,630 None
ANVISA (Brazil) 173 3
DAV (Vietnam) 51 None
MINSA (CR) 8 None
INFARMED (PT) 5 None
US FDA 4 1
MFDS (Korea) None 2
EMA None 1

Questions about Pharmascience

Does Pharmascience hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Pharmascience. It does have 1,883 filings with 13 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Pharmascience FDA-registered?
One site operated by Pharmascience 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.
How did Pharmascience's last inspection go?
The most recent inspection on record closed on 13 February 2024 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 5 inspections are on file.
Where does Pharmascience manufacture?
4 registered sites are on record, in United Arab Emirates, Brazil, Canada and Cyprus (Montreal, Betim and Canada among others). Every site is listed on this page with the register it came from.
Which regulators recognise Pharmascience's GMP?
Current GMP certificates are on record from ANVISA (Brazil), MFDS (Korea), EMA and US FDA. 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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Open risk flags

  • The most recent inspection outcome was VAI, on 13 February 2024.

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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