WHO WE ARE
We are integrity-based professionals from various technical, scientific, engineering, operational, and regulatory backgrounds with decades of experience in GMP-regulated industries such as innovative pharmaceuticals, biologics development and manufacture, generics and medical device industries.
WHAT WE DO
We are consultants to the regulated life science industries.We help clients achieve and maintain full compliance with Health Canada, FDA, EMEA and WHO regulatory requirements. Our consultants facilitate commercialization of your new products and help you interface with various agencies to address regulatory concerns.
WHERE WE WORK
From our headquarters in Montreal – Canada, our consultants provide services to firms across the Americas, Europe, Asia and the Middle East.
Our multicultural and multilingual professionals are uniquely positioned to optimize collaborations with your teams, no matter where you are located.
QUESTIONS ABOUT A PHARMACEUTICAL ISSUE? ASK OUR EXPERTS.
INTERNATIONAL
Lesirg Consultants enjoy strategic collaborations with quality auditors, consultants, and professionals in key regions of the world allowing seamless project transition, and team integration.
COMPREHENSIVE
Lesirg Consultants assist organizations across several aspects of their operations.
From innovative and strategic analysis to cross-functional operational assistance and quality compliance.
EXCELLENCE
Because of our flat organizational structure, our consultants enjoy unparalleled freedom of operations, resulting in a deeper engagement with our clients, from both technical and human aspects.