Our Consulting Services

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With a wealth of experience in drug development, our consultants are here to guide you through every stage. We focus on your unique needs to ensure a successful path to market. Led by board-certified subject matter experts, we deliver customized solutions that align science, operations, and business goals.

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From preclinical studies to toxicology assessments, we offer comprehensive non-clinical support tailored to your specific needs. Our experienced professionals will help you design and execute studies that meet regulatory standards and advance your drug development.

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Our Global Monitoring service ensures seamless oversight of clinical and development activities in Canada, and across multiple geographic regions (including North America, Asia, India, Australia). With an emphasis on quality, consistency, and compliance, we coordinate and supervise studies conducted internationally to maintain alignment with regulatory standards, protocol integrity, and sponsor expectations.


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Our regulatory affairs experts are dedicated to helping you navigate the complexities of drug approval. We provide insights and strategies to ensure your submissions are thorough and compliant, reducing time to market.

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Clear, accurate, and regulatory-ready communication is at the core of successful drug development. We transform complex data into compelling, compliant documents that support every stage of your program—from non-clinical summaries and clinical study protocols to regulatory submissions and publications.

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Our PK/TK modeling services provide critical insights into a drug’s absorption, distribution, metabolism, and excretion (ADME) profiles to support data-driven decision-making throughout development. By applying advanced modeling and simulation techniques, we help predict human dosing, optimize study design, and assess safety margins with confidence.

VJO Canada's Unique Drug Development Model

Optimizing Your Path to Success

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At VJO Canada, we understand that every biotech company has unique challenges and goals. Our innovative model for drug development consulting is designed to streamline processes and enhance efficiency, ensuring that you stay on track towards your exit strategy.

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Our approach is rooted in the philosophy of reverse engineering. By starting with your end goals, we customize the entire research process to optimize performance and deliver results within your specified timeframe.

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We leverage a robust project management framework and a regulatory compliance management system to minimize overhead costs and accelerate milestone delivery. This allows you to focus on what matters most:


streamlining your drug development program.

Tailored Strategies for Every Stage

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From non-clinical proof of concept to Phase 2 readiness, our multidisciplinary team of experts is equipped to support you at every stage of drug development. We prioritize efficiency and effectiveness, ensuring that your project remains on the critical path.
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Our seasoned professionals, with over 100 years of combined experience, bring invaluable insights from big pharma and biotech. This expertise enables us to navigate complex challenges and drive your program towards successful outcomes.
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Collaborative Partnership

At VJO Canada, we believe in the power of collaboration. We work closely with our partners to understand their specific needs and tailor our services accordingly, fostering a partnership that enhances the drug development journey.

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Our commitment to excellence is reflected in our proven strategies that achieve significant cost and time efficiencies. By optimizing logistics and performance output, we ensure that your project is not only successful but also sustainable.
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Join us in transforming your drug development vision into reality. With VJO Canada as your partner, you can navigate the complexities of the industry with confidence and clarity.
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Let’s work together to accelerate your path to market.