Our medical regulatory company offers three unique solutions to expedite your device and drug approvals globally.
Obtain instant access to the most up-to-date medical device regulations and actionable intelligence for over 100 markets worldwide.
Leverage our extensive network of over 4,000 vetted regulatory consultants to get verified answers to your most critical compliance questions.
Monitor global regulatory changes in real-time to avoid risky surprises.
Join the list of industry-leading companies
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We can help you expand to any market in the world.
Medical device and pharmaceutical companies spend months gathering intelligence from disparate sources and preparing product registration submissions, oftentimes only to be rejected by health authorities. RegDeskTM as medical regulatory company solves that problem.
Coverage of over 100 markets and management assistance for product approvals in each and every one
Utilization of artificial intelligence to deliver the most valuable and updated regulatory insights
Constant monitoring of global regulatory changes
Use of crowdsourcing to find answers to the most pressing regulatory questions
Instant access to accurate and competitive regulatory intelligence
Reduce time to market and risk levels to provide advantages over competitors