Manufacturing Expertise in Class I, Class II, Class III, Drug-Device combination products and more.
Experience working with 13 global regulatory bodies including the FDA & EMA.
Expertise in QMS Development and Optimization, Risk Management, Technical Documentation and more.
At LaSalle we have worked with over 100 business units/organizations in 14 countries. Although the majority of our work supports biotechnology, biopharmaceutical, and medical device manufacturing sites, we have also worked with non-GxP manufacturing, Healthcare, Technology and Financial institutions.
We work at both corporate and site levels. Our team has engaged organizations with fewer than 30 people, manufacturing sites ranging from 30 to 5,000+ employees, and Fortune 500 companies with over 100,000 people.
The median professional experience of our consultants is 25 years. Our handpicked team was built to provide you with the strategic, execution and technical expertise required to support you and your team. In essence, you will likely spend the bulk of your time interacting with former Director-Level and higher ranking experts with a hands-on, people focused vision - not junior staff.
Most of our consultants spent their careers as in-house leaders running regulated manufacturing sites. That experience shapes how we work. We understand the operational, financial, and regulatory pressures your team faces so we provide hands-on, execution support. We deliver results, not just roadmaps.
Let’s talk about your goals, challenges, and the right path to measurable results.
