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WHO WE ARE

Challenging ourselves to bring innovative and quality solutions

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Lesirg Consultants Inc. is a dynamic consulting firm specialized in providing QA, compliance, regulatory, project management and productivity improvement services to the pharmaceutical, biotechnology and medical device industries.

Our consultants are seasoned professionals from various technical, scientific, and regulatory backgrounds with decades of collective experience in GMP-related industries. Our focused approach in providing real time and customized services to our clients has proven to be both effective and cost efficient.

We provide services to firms across the Americas, Europe, Asia and the Middle East

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WHAT WE DO

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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.

In addition to providing strategic and management consulting services, we bring technical expertise in quality assurance, project management & facilities commissioning, productivity & efficiency improvement, outsourcing & supply chain management, validation, and regulatory compliance.

WHERE WE WORK

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From our offices in Canada and the United States, 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.

Lesirg Consultants enjoy strategic collaborations with quality auditors, consultants, and professionals in key regions of the world allowing seamless project transition, and team integration.

Ask One of Our Experts!

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We’re here to help answer your questions. Pharmaceutical matters can be complicated, our experts are on hand to help inform you of every aspect regarding your topic.

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