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Introducing a fully managed, expert-led literature review service for regulated industries, academic research, and non-profit initiatives.
ECNE SafeSearch Pro delivers tailored, audit-ready insights from the global scientific literature to support strategic, regulatory, and evidence-generation goals.
Whether you're monitoring for emerging safety signals, supporting PMCF activities, preparing for regulatory submissions, defining your product's state-of-the-art, or generating credible insights for clinical practice, policy, advocacy, or grant-funded research; SafeSearch Pro provides a trusted, scalable solution.
Empower your clinical, regulatory, and medical teams with high-quality, actionable intelligence - without the overhead.
A fully-managed, expert-led literature review service, combining clinical precision with zero effort required from your internal teams.
SafeSearch Pro combines expert oversight with software-enabled precision, giving you clean, actionable evidence with zero internal lift.
Who Is It For?
✔ Pharma & Biotech Teams
✔ Medical Device and In Vitro Device Teams
✔ Regulatory Teams
✔ Medical Affairs Teams
✔ Nonprofit & Academic Researchers
Expert-led and entirely managed, our literature review service ensures clinical precision, without adding to your team’s workload.
✔ Up to 25 data points extracted per product
✔ Delivered quarterly, biannually or as a one-time engagement
✔ Fully auditable, scalable, and compliance-focused
Shannon, Director of Clinical Affairs
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