A fully managed, tailored AI-enhanced literature service that combines advanced search, screening, and data extraction capabilities with expert-in-the-loop oversight. This service provides actionable intelligence, ensuring that outputs are customized to meet your specific needs while adhering to regulatory standards.
Trusted by clinical, regulatory, and medical teams, SafeSearch Pro™ offers a blend of expert oversight and software-enabled precision to deliver insights from the global scientific literature, supporting your strategic, regulatory, and evidence-generation goals. Our outputs are regulatory-ready and integrate seamlessly with your Quality Management System (QMS).
Who is it for?
- Pharma & Biotech
- Medical Affairs Teams
- Regulatory Affairs Teams
- Medical Devices and In Vitro Devices
- Pharmacovigilance and Safety Teams
SafeSearch Pro™ stands out by combining human clinical oversight with AI-enabled automation, regulatory-aligned methodology, structured extraction, and submission-ready formatting. This results in tailored, regulatory-grade intelligence delivered at scale, alleviating the internal burden.
ECNE Research has been selected to present at ISPOR 2026, sharing new evidence on expert-guided AI workflows for systematic literature reviews and demonstrating their role in providing high-quality evidence more efficiently.
