1,000+ of the world's leading MedTech companies trust Greenlight Guru.
Pre-Validated Post-Market Surveys
Don’t risk your device’s market position with flawed post-market data! Ensure optimal and compliant post-market survey data with minimum effort and resources. The SMART-TRIAL Survey tool comes pre-validated per ISO 14155:2020 and enables GCP compliance out-of-the-box. All to help you set new standards for your post-market data quality.
Get your Post-Market Surveys Right!
We’ve built the ideal post-market survey tool for your device, so you can focus on improving the quality of life for your patients.
Maintain Data Overview
Integrate your post-market survey data with the SMART-TRIAL by Greenlight Guru platform and manage all your data collection in one system.
Fast to Set up, Easy to Repeat
Set up your post-market survey easily with our intuitive study builder, and clone and repeat your surveys infinitely.
Never worry about data origin validation again! All data inputs automatically include automatic user identification to ensure full traceability from source to sponsor.
Simplify Clinical Data Compliance
SMART-TRIAL Survey is pre-validated and compliant with ISO 14155:2020 requirements, enabling you to easily collect GCP compliant post-market surveillance data. Additionally, SMART-TRIAL Survey simplifies compliance with MDR, FDA CFR 21 Part 11, GDPR, and more.
Post-Market Surveys Shouldn’t Be Hard
Designed to streamline your entire post-market clinical data collection process, minimizing time and resources needed to ensure consistent, high quality data.