Accessing Your Target Market: Introduction to Key Regulatory Requirements
Time & Location
About the Event
Medical technology continues to advance, new innovative therapies are coming from applied research activities, and patient care opportunites expand worldwide. Matching your medical innovation to the right initial, or next, market opportunity is key to moving to the next phase of adoption. Understanding the strategic implications of the market choices, grasping the business consequences of that choice, and developing a knowledge of the regulatory, quality and clinical environments into which you wish to launch will all be critical to successful outcomes. This webinar will introduce you to these important topics and decision points.
This webinar will provide an overview of:
- Some of the key topics to consider with regard to the target market for your medical device and the regulatory, quality and clinical implications that follow from that choice.
- A brief overview of the EU, UK & USA markets with some information on the rest of the world.
- Tools to utilise in determining the potential regulatory approach to take for your proposedtarget market.
- Key practical considerations as you move forward with the design and development,production and marketing of your device.
Target audience: Manufacturers & developers of medical devices entering the market for the first time or looking to grow into a new market opportunity. Medical Technology Entrepreneurs, Medical Device Developers, Technology Transfer Officers, Medical Technology University Researchers, IVD Developers, Business Owners, Executives, Product Owners, Regulatory Specialists within a company that need to understand, from a strategic perspective, the overall regulatory requirements for their medical devices in new target markets. All company sizes will find it useful.
SPECIAL OFFER - BOOK BOTH WEBINARS:
SEHTA member - £230 + VAT Non-member - £280 + VAT
Price for one webinar:
SEHTA member - £130 + VAT Non-member - £150 + VAT