Date: Thursday, March, 26, 2026
Time: 16:00 - 17:00 CET | 10:00 - 11:00 am EDT
Location: Virtual
Introduction
For many MedTech founders, navigating regulatory requirements can feel like the biggest obstacle to getting innovative products to market. But the truth is, understanding those regulations early can be one of your strongest competitive advantages. In addition, many other aspects of building a medical device business require vast knowledge and experience for success.
In this joint session, experts from QuickVault by Veeva and Qserve Group explore how education around a MedTech company’s journey empowers startups to operate efficiently, stay compliant, accelerate time to market, and reach commercial success.
Learning Objectives:
We’ll share practical insights on:
- How to identify the essential areas of regulatory knowledge for early-stage teams and how to apply them in your day-to-day activities
- When and how to leverage external experts effectively
- How regulatory understanding can fuel better operations, faster execution, and investor confidence
- The various ways teams can acquire knowledge (through education, mentorships, joining MedTech companies etc.)
If you’re building or supporting a MedTech startup, this conversation will show you how knowledge and compliance can become your fastest path to impact.
Who should attend?
This webinar is designed for anyone involved in building, scaling, or supporting early-stage MedTech ventures, including:
- Founders and co-founders who want to de-risk their product journey and avoid costly regulatory surprises
- Startup leadership teams (CEO, COO, CTO, Head of Quality/Regulatory) seeking practical ways to integrate compliance into daily operations
- Product and engineering leaders who need clarity on how regulatory requirements impact development timelines and decisions
- Investors, incubators, and accelerators supporting MedTech companies and aiming to strengthen portfolio readiness
- Early regulatory or quality professionals looking for a strategic view of how knowledge accelerates execution, not just compliance
If you’re responsible for turning MedTech innovation into a market-ready product, this session will help you understand how the right regulatory knowledge can become a competitive advantage.
Agenda
- Welcome
- Introduction - Axel Strombergsson (Veeva QuickVault)
- Regulation overview, what most common regulations and standards you need to have knowledge of (MDR, 21 CFR 820, ISO 13485, ISO 14971) - Robert Paassen (Qserve Group)
- Access to other knowledge: mentors, accelerators and incubators - Axel Strombergsson (Veeva QuickVault)
- Efficient operation for product development and speed to market - Axel Strombergsson (Veeva QuickVault)
- Live Q&A