• 2016
    • Build of second  cGMP manufacturing site in Canada
    • cGMP  manufacturing in Ireland
  • 2015
    • Health Canada Licensed for API manufacturing, labeling, testing and distribution
  • 2014
    • EXCiPACT Certification, first excipient manufacturer in North America to receive the accreditation
    • FDA registration completion for pharmaceutical ingredient manufacturing
  • 2012
    • ISO Certification
  • 2011
    • Completion cGMP facility renovations and GDP warehousing
    • Launch A&C USA and opening of sales office
  • 2008
    • Hosted first Ph. Eur. 6th Edition training session in Canada with the EDQM
  • 2007
    • Start of building expansion and upgrade towards cGMP environment for our existing and new excipient product range
  • 2006
    • Hosted first USP Educational forum Conference in Montreal
    • Successful registration of USDMF for Azelastine HCL with FDA –  FDA Audit/DMF review / Manufacturer approval
  • 1990
    • Plant expansion, doubling production and warehousing due to new buffer and cleaning solution product range
  • 1975
    • Distribution of USP Reference Standards, making us the oldest USP distributor worldwide
  • 1966
    • New Facility built In Montreal due to increase in sales and new product development