Accurate. Accelerated. Approved.
Cardinal Health Regulatory Sciences delivers proven regulatory consulting expertise to help you obtain global product approval and maintain filings throughout the entire product lifecycle.
Unmatched regulatory consulting expertise
Every day your therapy sits in the development pipeline, you lose money, and patients lose the opportunity for treatment. That’s why it’s critical to get your regulatory strategy right the first time, every step of the way.
Cardinal Health Regulatory Sciences will partner with you to develop the best regulatory pathway for your product, through every stage of its lifecycle. Our regulatory strategies can reduce the risk of failure, and increase your speed to market.
Experience you can trust
Over the past four decades, our team of 200+ industry-trained regulatory consultants has provided expert guidance to help pharmaceutical, biotech and medical device companies get their products to market quickly.
Our regulatory consultants average more than 18 years of industry experience, many have worked at the FDA, and more than 65% have advanced degrees.
A track record of success
We’ve successfully worked with global regulatory agencies and every review division of the FDA. We’ve provided drug development services for new drugs in all major therapeutic areas, and have experience working across more than 175 countries. Our dedicated client service teams help to ensure projects stay on track, and on time. Let us put our proven regulatory consulting to work for you.
Learn more about our Regulatory Consulting Services.
Learn how a VC-backed therapy was lifted off FDA clinical hold
Accelerating approval for cell and gene therapies
