Meeting your compliance objectives in a world of constant change and financial challenges means doing things differently. It requires automating, adopting advanced technologies, and leveraging outsourcing.
Our innovative pharmacovigilance (PV) solutions are powered by the IQVIA CORE -- integrated, scalable technologies combined with global data, advanced analytics, and deep domain expertise. Helping you predictably and cost-effectively achieve your safety and surveillance goals.
ANNETTE WILLIAMS, R.Ph, VP, Pharmacovigilance, IQVIA
Technologies such as artificial intelligence (AI), machine learning (ML), and Natural Language Processing (NLP) are transforming today’s resource-intensive pharmacovigilance workloads, ensuring a more informed, more efficient approach.
Tracking adverse events is just one of your mission-critical responsibilities. But the number of sources to look at is rapidly expanding, from your own digital and social media properties, to public web data and regulatory sites. Sifting through all those sources can be so resource-intensive that it leaves little time for anything else.
AETracker replaces labor-intensive monitoring and tracking of these adverse event data sources with sophisticated AI and automation. Platform-agnostic, this turnkey solution easily integrates into existing drug and device safety workflows.
Complex requirements screening of data is backed by 100% human verification to ensure that safety gets a manageable list of suspected AEs on a timely basis.
IQVIA's safety group also offers functional, operational and technical expertise in each geography, executed by integrated local teams that meet a range of time zone and language requirements. We handle hosting and safety management services via 16 validated, state of the art SSAE data centers designed with security, ﬂexibility, scalability and vendor neutrality in mind.
Our pharmacovigilance business is one of the largest groups of PV experts worldwide, with a combination of deep life sciences expertise and best-in-class technologies. So you can expand your pharmacovigilance and safety capabilities with confidence - and without additional capital investment.
Automate and standardize your regulatory management, from correspondence and commitments to registration and tracking.
From manufacturing oversight to regulatory requirements, manage quality across your organization with a single enterprise software solution.
Proactively address global engagement and transparency regulations with technology solutions that streamline and simplify processes, reduce costs, mitigate risks, and leverage data.
Use AI, machine learning, NLP and new technologies to streamline pharmacovigilance, improve efficiencies, reduce costs, and meet safety demands.