The Validant Difference
We’ve solved diverse problems across the entire GxP lifecycle. We apply that experience and our wide range of capabilities to deliver specific, customized strategies alongside execution resources to meet your requirements—anywhere in the world.
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We exclusively serve pharmaceutical, biologics, medical device, and diagnostics developers and manufacturers seeking to bring to market and commercialize products globally.
As former industry leaders and health agency regulators ourselves, we understand your need to balance the real-world realities of running a business with reducing exposure to regulatory risks. We bring pragmatic perspectives and a long track record of solving complex regulatory, compliance, and quality challenges — as well as proactively strengthening quality while keeping costs in check.
Validant’s platform is highly unique in that in brings together specialists across the full GxP lifecycle, from preclinical and clinical phases to manufacturing and distribution. You gain the efficiency of working with one partner that has the expertise to ensure the compliant progression of your product from end to end.
Validant’s team applies their deep and diverse knowledge, which remains in lock-step with evolving global standards and regulations, to customize an action plan around your specific problem or need.
Unlike a traditional bench model, Validant’s capacity is nearly unlimited in terms of project size and global reach. That is because we have carefully curated a large global network of consultants with diverse technical credentials and regional- and language-specific skills.
This gives us the unique ability to build a team or teams to the right size, with the right level of expertise and cultural fit, in the right locations rapidly. All talent is hand-picked and managed by a Validant partner to ensure our high quality standards are maintained.
We know that when regulatory, compliance, or quality issues arise, time is of the essence. Our flexible model enables us to deploy teams from 1 to 100+ rapidly — even in as little as a week.
This speed is critical to address pressing compliance infractions but also invaluable in implementing proactive initiatives that will keep you ahead of changing standards and your competition.
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