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A custom-designed platform that converts the tedious task of sending drug safety reports into easier steps, clearer tracking, and more connected workflows. At the same time, this advanced system helps reduce the deluge of unnecessary safety reports and makes safety reports more searchable and meaningful to investigators.


­TriPort® Trial Portal makes it easy and intuitive for study teams, CRAs, and investigators to rapidly complete a variety of safety report tasks.


Supports DILs, Initial SUSARs, Follow-up SUSARs, New Safety Findings, Semi-Annual Safety Reports (SASR), and other Safety Reports.


Automated rule-based distribution according to regulations by country and the characteristics of individual safety reports, effectively eliminating unnecessary reporting burden.


Use for single studies or across a multi-study development program, with one-time document upload and distribution, and one-time eSignature completion by investigators across multiple studies.


Clarity of design allows study teams, CRAs and sites to view and track completion of safety reports at the individual site or study level, with graphical displays and automated reporting.


Automated exchange of documents and data with pharmacovigilance safety systems, for improved quality and seamless, expedited workflows.


Easily search according to multiple criteria, including adverse event category, country, date, type (SUSAR, New Safety Finding, SASR, etc.), and relatedness (initial and follow-up SUSARs).


Single Sign-On to one platform with training, study documents, correspondence, FAQs, patient visit guides, searchable protocol, site engagement and more.

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Manage user access by role and location, with automated archiving and audit trails, in a compliant, validated document repository.

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