Clinical Regulatory Services
Together, we’ll plan a strategy and execute it to give you the best chance of regulatory approval.
Regulatory Approvals Go More Smoothly with the Right Partner.
Our end-to-end solutions take you from strategy, audit, submission, publishing and post-licensing support
Your team includes over 150 regulatory affairs professionals in more than 14 countries
Your regulatory experts bring up to 30 years each working with regulatory processes
It’s not easy to navigate all clinical regulatory needs. An experienced ally can get you there.
Your product needs an innovative regulatory strategy. That’s what we’re here for. Our team members each have 15–30 years of drug development and regulatory experience and we put it all to work getting you where you need to be, faster. Together, we reveal how your target product profile impacts decisions on study design, location of patient recruitment and future registration interests.
You want to see the big picture, while understanding market-to-market realities.
We bring global regulatory experience home. Our regional expertise and strong relationships with health authorities in Asia Pacific, North America, Latin America and Europe mean smooth sailing for your strategy.
You’re looking for someone on the ground that appreciates an ever-shifting landscape.
Covance will help you develop insightful responses to ever-changing local and federal regulations. As your advocate at advisory meetings, trade associations, scientific conferences and state regulatory conferences, we help you navigate regulatory environments around the world.