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, since many 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.
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.

QuickVault by Veeva is the leading device-to-market solution for MedTech companies. Built for full device lifecycle support, the platform unifies design, regulatory, quality, and post-commercial operations in one scalable environment, helping teams stay agile, compliant, and ready to grow.
From concept through commercialization and beyond, QuickVault by Veeva gives MedTech companies the visibility and control they need to deliver safe, effective products to patients and succeed at every stage.

Qserve is a trusted global partner for MedTech Regulatory, Clinical, and Quality Compliance, as well as a full-service CRO for medical device clinical trials.
With a strong international presence in Europe, China, and the United States, our team of experts combines deep regulatory knowledge with hands-on industry experience to help manufacturers achieve global market access for all types of medical devices and in vitro diagnostics (IVDs).