FREE ON-DEMAND WEBINAR
Behind the Stats: 2020 State of Medical Device Product Development & Quality Management Benchmark Survey
The balancing act of documenting the right things and staying up-to-date with the ever-changing regulations is a commonly shared challenge amongst medical device product development and quality teams.
To help paint a picture of the strategies, tactics, and technologies used today by medical device professionals to accelerate product development, ensure compliance, and promote quality, we conducted an industry benchmark survey that's culminated in the 2020 State of Medical Device Product Development and Quality Management Report.
Key findings of the report include:
- 75% of medical device professionals are unprepared for an unannounced audit
- Key challenges to improving product development processes include:
- Resource constraints: 55%
- Lack of budget: 37%
- No management support: 29%
- 71% of respondents indicated they do not currently have easy, real-time access to quality system data
- Additionally, nearly 60% of professionals noted that quality system data isn’t consistently reliable
This free in-depth webinar, presented by Greenlight Guru founder and VP of QA/RA Jon Speer, will dig deep into the report findings of over 500 medical device professionals around the globe, to share the most compelling stats, biggest surprises, and must-know takeaways device makers need to know.
You'll gain valuable data-driven insights into how companies are currently managing their product development and quality activities, as well as what makes or breaks a market leader so you can learn what you need to do to rise to the top in 2020.
Watch the webinar
Specifically, this webinar will cover:
- Data driven insights on key markers for success
- Identified traits of medical device market leaders
- Key challenges faced by medical device professionals
- Strategic roles of product developers and quality managers in driving company growth
- Proven strategies, tactics, and technologies to manage product development and quality activities
- Current landscape of quality management solutions and tools
- Q&A Session
Who Should Attend?
- Medical Device Executives
- Regulatory Affairs Professionals and Management
- Quality Professionals and Management
- Clinical Affairs Professionals and Management
- Product Development & R&D Engineers and Management
About Greenlight Guru
Greenlight Guru is the only quality management software platform designed specifically for medical device companies. The platform helps companies bring safer products to market faster, simplifies FDA and ISO regulatory compliance and provides a single source of truth by connecting the management of all quality processes like CAPAs, risk, audits and more. Greenlight Guru’s platform is used by thousands of users across the globe to push beyond baseline compliance and achieve True Quality for their medical devices.
