Adverse Event Management
We start with an attitude that drives a philosophy — every case matters. Whether volume levels are high, involving a well known commercial brand or simply a few individual cases associated with a new compound, we treat them with the same meticulous attention to detail. Our belief is that every case is a reference point for decision making. At Sentrx, helping you make the right decision is our primary motivation.
Your challenge is to gain the insights you need to extend safety into commercial value. We understand. Sentrx can help you balance quality adverse event management with operational imperatives by making costs variable, adding flexibility, or supporting global reporting and partnering. We provide complete business process outsourcing or just the aspects you need, such as specific functions or work-steps. We’ll customize the adverse event management process you need now and change it as you grow.
Sentrx has handled adverse events in virtually every therapeutic area and produced solutions in situations ranging from rapid launch support to crisis management. We routinely address issues such as global serious adverse event centralization, Phase IV survey assessment, and complex data migration problems.
To achieve your pharmacovigilance goals accurately, effectively, and efficiently, Sentrx brings the right technologies to bear. In addition to drug safety systems, for which we are a world-class ASP host, Sentrx offers proprietary software tools to ensure efficient workflows and streamline processes, such as dictionary updates. To maximize flexibility, Sentrx offers multiple options to boost efficiency and reduce costs.
We know what you need — adverse event management customized for you, integrated to the way you do business, and scalable to meet changing dynamics. For adverse event management solutions, talk to Sentrx.
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Adverse Event Management At A Glance
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Doreen Lechner, PhD EVP Pharmacovigilance Client Services |
