Regulatory and Quality Consulting for Medical Device Manufacturers
Navigating Compliance, Empowering Success
Explore our range of services, from regulatory pathway analysis and risk assessment to market launch optimization. Let us be your partner in transforming regulatory challenges into strategic opportunities.
Lucora will elevate your medical device's regulatory journey into a launchpad for success.
It serves as a constant reminder of the people and families that are served by advances in healthcare.
“Lucora” blends the names of the founder's children.
What People Are Saying
"Working with Lucora was a game-changer for us. Their insightful regulatory consultants went beyond the norm, considering multiple markets while crafting our design verification testing strategy. This approach not only ensured compliance but also saved us tens of thousands of dollars by having the foresight to avoid redundant testing due to minor regional variations. Their holistic perspective is a rarity in the industry and undoubtedly fueled our success."
- E. G., President of Technology
"We were unsure about bringing on a consultant since we had an in-house regulatory staff. [The Lucora team] was brought on to help chip away at a backlogged project. She took the time to understand our device, SOPs, and risk tolerance and respectfully suggested ways to improve our efficiencies. Implementing the solutions proposed by [Lucora] streamlined our day-to-day in a way we never thought possible. A way we never thought to ask for. We certainly got more long term value than we expected."
- R.K., RAQA