The Immersive Experience Product: Innovating to Win in Digital Sales
Three Key Tools from the Diagnostics Industry that will Become the “Radar” in the War Against Pandemics
How Low-Demand Design is Poised to Triumph in Home Health
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...
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