During this session, featured speaker Brandon Bogdalek, will interview three industry leading panelists. The panelists will discuss important factors to consider when evaluating off-the-shelf (OTS) drug delivery platforms vs. developing a novel solution. Key topics...
Drug Delivery – Evaluating Off-The-Shelf and Novel Drug Delivery Solutions
During this session, Brandon Bogdalek will interview three (3) panelists from in the drug delivery and pharmaceutical industry. The panelists will discuss important factors to consider when evaluating off-the-shelf (OTS) drug delivery platform vs. developing a novel...
Embracing Human-Centered Design to Create Impactful Digital Experiences
During this session, Brandon Bogdalek will interview three (3) panelists in the pharmaceutical industry. The panelists will discuss how to use human-centered design principles and techniques to create digital experiences that patients love. In a world where digital...
Best Practices for Bringing Novel Point-of-Care Diagnostic Solutions to Market
During this session, Brandon Bogdalek will interview three (3) panelists in the diagnostics industry. The panelists will discuss best practices for bringing novel point-of-care diagnostic solutions to market. The audience will hear from founders, CEOs, and executives....
The Innovation Imperative for Growth Stage Medical Technology Companies
During this session, Brandon Bogdalek will interview panelists from the medical technology space. The panelists will discuss the innate need to innovate as a growth stage company, and the different strategies used to bring differentiated products to market. The...
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...