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How Software Can Be Leveraged To Speed Your Time to Market and Reduce Risk
On average, it takes between 3 - 7 years for a new medical device to go to market with FDA clearance or FDA approval.

As a MedTech startup founder with limited runway and resources, you need your time to market to be as fast as possible. At the same time, to ensure the safety and efficacy of your device, you have to stick to certain quality standards.

Finding the right balance between getting into the market as quickly as possible and maintaining quality standards can be very tricky.

That's why Dreamit and Greenlight Guru teamed up to host a webinar that teaches MedTech founders like you how to use software to speed your time to market in a safe and compliant way.

In this webinar, Greenlight Guru's MedTech experts will cover:

- How to accelerate product development efforts — from napkin idea, to 510K approval, to market release — by months or years

- How to manage risk to drive the safety and quality of products and processes through QMS per ISO 13485:2016 & 21 CFR Part 820

- How to change your company’s focus from simply meeting regulations to building quality into your processes as a differentiator

- How to understand and stay ahead of the FDA and EU changing quality regulations as leaders instead of followers

Register for the webinar today to ensure your medical device startup has the best chance to succeed.

Jan 24, 2019 1:00 PM in Eastern Time (US and Canada)

Webinar is over, you can not register now. If you have any questions, please contact Webinar host: Dreamit Team.