Pillar5 Pharma’s New QM System

SOLABS announces corporate go-live of SOLABS QM at Pillar5 Pharma Inc.

SOLABS and Pillar5 Pharma Inc. are delighted to announce the corporate-wide go-live of the SOLABS QM Quality Management Software at the Pillar5, Arnprior, Ontario, manufacturing site. Since its inception in 2009, Pillar5 has continued to carry on the legacy of the former Pfizer manufacturing site, striving to remain innovative and forward-looking in finding new ways to better serve their clients. The system, which went live this June, will help the company better manage their Quality Documents and improve their Change Control Processes.

“We are very proud of our continuous success in projects such as the Pillar5 implementation. We pride ourselves on offering a total solution to our clients. Our teams worked very closely in making sure the specifics goals of this project were met in a timely matter”. (Valerie Paradis, COO at SOLABS).

“The implementation of this software has allowed us to expand on lean initiatives within our organization by consolidating multiple extensive processes into one easy-to-use, GMP compliant system. We are also excited about the expandability of the software, as a means to further growth and added value for our customers”. (Jamie Moore, Director Quality Operations at Pillar5).

About Pillar5 Pharma Inc.

Pillar5 Pharma Inc. a Contract Manufacturing Organization (CMO) established in December 2009 further to the acquisition of the former Pfizer facility in Arnprior, Ontario, Canada. This plant has been in operation since 1956 with significant investment in equipment, processes and people over the many years of successful operations.


SOLABS has been a market leader in Canada by deploying best in class Quality solutions exclusively to the Life Sciences market for more than 10 years. SOLABS delivers a complete solution including software, services and support in a simple, cost-effective manner. The integrated SOLABS QM software solution helps improve Quality operations and processes, and provides critical compliance to 21 CFR part 11 and other regulatory requirements. The solution has proven to be easy to use, operate and maintain.