Trust Med Communications’ Pharmacovigilance Experts for Regulatory Information Specific to Your Needs

With the world of life sciences changing almost daily, navigating information overload in the pharmacovigilance space and keeping abreast of all relevant regulatory information has become critical — and increasingly difficult — for pharmaceutical companies. New and important information on various drug safety areas can be found in many scientific resources around the world, including government email alerts, e-newsletters, pharmacovigilance/regulatory blogs, professional societies’ websites, scientific events and conferences, regulator’s RSS feeds, public hearings, and advisory committee meetings. A competent and experienced regulatory intelligence group can design a regulatory strategy based on a thorough and continuous analysis of existing and new information coming from these and other sources, allowing organizations to identify relevant regulatory trends, streamline the effort of their internal departments, and become familiar with the hot topics usually quoted by regulatory authorities during inspections.

To ensure compliance, Med Communications’ team of pharmacovigilance experts can work through the information overflow to capture the pertinent information based on a company’s business priorities, all while supporting an aligned understanding of applicable requirements. For pharmacovigilance regulatory guidance tailored to your needs, please contact us: 877-477-0977 or

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