Global Literature Review: Ensuring Safety through Robust Processes

Learn how our end-to-end GLR process enhances patient safety and supports regulatory compliance worldwide.

In pharmacovigilance, timely identification of safety signals is essential to protecting patients – which is why our Global Literature Review (GLR) process provides a systematic and reliable way to capture, analyze, and document safety data from trusted scientific sources like Embase and PubMed.

With tailored search strategies, advanced screening, and clear reporting practices, we help pharmaceutical companies ensure compliance while strengthening their safety surveillance.

Whether as part of a global pharmacovigilance project or a standalone service, our GLR process delivers precision, adaptability, and excellence you can trust.

Download our bulletin below to learn more:

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Global Literature Review: Ensuring Safety through Robust Processes

Pharmacovigilance outsourcing for boosting compliance and safety for biotech companies

Breaking the Silos Across Medical Information & Pharmacovigilance – Leveraging Technology for Operational Efficiency

Whitepaper: Computerised System Validation & Pharmacovigilance

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Big Enough To Cover All Your Needs.Small Enough To Care.

Clinical Research

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Quality Assurance

Global Literature Review: Ensuring Safety through Robust Processes

Pharmacovigilance outsourcing for boosting compliance and safety for biotech companies

Breaking the Silos Across Medical Information & Pharmacovigilance – Leveraging Technology for Operational Efficiency

Whitepaper: Computerised System Validation & Pharmacovigilance

Big Enough To Cover All Your Needs. Small Enough To Care.

Clinical Research

Regulatory Affairs

Pharmacovigilance

Medical Information

Clinical Trials

PV System & QPPV

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