We screen local, regional and non-English literature to capture safety information that global databases can miss, keeping your product's safety profile complete and compliant.
We monitor local medical and scientific literature to identify adverse drug reactions and ensure compliance with regulatory requirements.
Our pharmacovigilance experts provide in-depth analysis and reporting tailored to your needs.
Coverage of non-English and region-specific journals, databases and publications for a complete safety profile.
Ensuring all literature search activities meet local and global regulatory requirements and audit standards.
Delivery of customised literature search reports to support your pharmacovigilance and regulatory submissions.
Early identification of potential safety signals through systematic review of local literature sources.
Robust quality control and documentation practices to ensure audit readiness and regulatory compliance.
Ongoing support and collaboration with client teams for seamless integration of literature search findings into safety processes.
Talk to our pharmacovigilance experts about a solution tailored to your products, markets and regulatory obligations.