Adapting an Existing Laparoscopic or Advanced Energy Device for a Robotic Platform
Clinical Data Management (CDM) Can Make or Break a Study’s Success
Leveraging Medtech Innovation in Clinical Trials
Rebecca Ford, Director of Program Management, discusses how to Leverage medical technology and innovation in clinical trials to drive medication adherence, capture impactful data and keep patients engaged through the entirety of the clinical trial. This presentation...
Webinar: Leveraging FDA Clearance/Approval for Successful EU MDR Submissions
The transition phase to MDR (Regulation (EU) 2017/745) has been underway since mid-2020 and has introduced new requirements for medical devices. Experience gained with numerous Notified Bodies during this critical time has highlighted common pitfalls and areas where...
EU MDR: Compliance Requirements From a Vigilance Perspective
Companies attempting to comply with Medical Device Regulation (EU) 2017/745 (MDR), introduced in May 2021 for medical device certification in the EU are challenged by the complexity and scope of the requirements. It is important for medical device companies to...
Never Miss an Opportunity
Nothing is more expensive than a missed opportunity. With the power and expertise of Veranex, we can propel your product journey towards the correct path and help you navigate the best opportunity to accelerate speed to market.
Digital Healthcare: To Discovery and Beyond
We recently sat down with Gary Keeler, Director of Digital Experiences and subject matter expert, to discuss the vast opportunities that exist in the digital healthcare space and how Veranex can empower your novel innovation.
One Minute With the Expert
We sat down with Dr. Olivier Chevènement, DVM, PhD, Veterinary Surgeon and Study Director at Veranex to discuss comparative anatomy of the tricuspid valve, the mitral valve, and why they are important to understand.
What differentiates us? It’s our people
Hear from Brian Loushine and why our people can create great outcomes.