DistillerSR delivers a regulatory compliant, transparent, and audit-ready software solution for more efficient pharmacovigilance literature triage.
Facing an increasingly complex and ever-changing regulatory environment, leading medical device and pharmaceutical companies, service providers, and CROs have chosen DistillerSR software for their pharmacovigilance literature triage.
DistillerSR is a comprehensive solution that automates many of the manual tasks involved in the systematic monitoring and screening of medical literature, ensuring that your literature review process is completed as efficiently as possible.
Why Choose DistillerSR?
DistillerSR tracks all project activity and provides customizable data capture, workflow, and reporting to conform to your business practices. With DistillerSR, you’re always audit-ready.
Automate your manual processes and spend more time on the things that matter. DistillerSR provides prescriptive, customizable protocols that facilitate standardized processes and methods across your organization.
Full Text Document Management
Track and manage your full text document acquisition within DistillerSR, attaching documents directly to the associated reference in your dossier.
Global Team and Project Management
DistillerSR’s real-time dashboards and customizable reports let you monitor your entire portfolio and team to ensure that things are running smoothly.
With its secure, cloud-based platform, DistillerSR is always available, whenever and wherever your team members need it.
Whether you manage 5 or 50,000 product dossiers, DistillerSR provides a fully scalable platform that can easily accommodate unlimited users and has unlimited reference capacity.
Dramatically Faster Updates
Living product dossiers in DistillerSR make updates fast and easy. Simply upload the latest search results, use the de-duplication tool to remove the references you’ve already screened, and process only the new references. The new data is blended with the original data for inclusion in reports.