SMi Trial —Protocol
Compliance Management
for Site-Based Trials
SMi Trial —Protocol
Compliance Management
for Site-Based Trials
SMi Trial —Protocol
Compliance Management
for Site-Based Trials
SMi Trial —Protocol
Compliance Management
for Site-Based Trials






How will you manage clinical trials
and sites remotely?

How will you manage clinical trials
and sites remotely?

How will you manage
clinical trials
and sites remotely?

How will you manage
clinical trials
and sites remotely?

SMi Trial helps sponsors and CROs transition to online clinical trial management by facilitating global communication and monitoring of sites, circulating protocol training and study updates, and deploying comprehension assessments to identify the high-risk areas of your trials without requiring on-site visits.

ScienceMedia also offers protocol compliance management for decentralized trials, SMi TrialD.

 
Read our case study to learn how a
top 5 CRO used SMi Trial to reduce
protocol deviations.

Protocol Compliance
Management

SMi Trial mitigates clinical risk and decreases trial cost by optimizing study compliance throughout the lifetime of your clinical trial. Our just-in-time therapeutic and protocol training, risk-based assessments, and real-time analytics serve to elevate clinical competency, improve the power of your clinical data, and ensure patient safety.

In contrast to the current one-and-done training in clinical trials, SMi Trial provides online clinical trial management tools that can be integrated into your study workflow and accessed, monitored, and deployed throughout the lifetime of your clinical trial.

 

Protocol Training

Elevate and standardize site performance with custom multimedia training targeted to high-risk areas of your protocol

Just-In-Time Access

Fight the "forgetting curve" with online protocol and medical distance learning to ensure your study team is always prepared with mobile-enabled access from any device, anytime, anywhere.

Interactive Schedule of Activities

Centralize key study procedure instructions with an interactive visit-specific guide.

Maintain

Protocol Amendment Management

Deploy, track, and re-train staff on protocol amendments throughout the lifetime of your study.

Audit-Ready Reports

Report the training completion of your study team with printable, audit-ready training records.

Study Updates

Share key lessons with custom updates targeting knowledge gaps discovered during the execution of the study.

Virtual Investigator Meetings and Site Initiation Visits

Reimagine traditional IMs and SIVs with remote pre-training, self-paced micro learning, standardization, and assessments. Access our webinar to learn more.

Maintain

Real-Time Analytics

Evaluate site staff competency in real time using role-based analytics on training status and comprehension.

Integrated Assessments

Identify knowledge gaps and activities at high risk of deviation and ensure compliance with ICH E6(R2) using protocol-specific training assessments.

Maintain

Interactive eLearning Incorporates:

  •    Protocol Essentials
  •    Product Overview
  •    Disease State
  •    Standards of Care
  •    Assessments
  •    Content Extensions

The Pillars of SMi Trial:

Targeted Clinical Risk Mitigation

Our clinical experts work with you to identify high-risk areas of your protocol to develop online targeted training and assessments. Real-time analytics provide visibility into training comprehension in order to identify knowledge gaps before they lead to unplanned protocol deviations.

Improve the Power of Your Clinical Data

The prevention of unplanned deviations ensures the reliability of your clinical data and minimizes the loss of usable subject data, resulting in decreased operational costs and expedited time-to-market for life-saving therapies.

Elevated Clinical Competency

Standardize site performance and minimize the impact of staff turnover with just-in-time therapeutic and protocol-specific training targeted to high-risk areas in your trials.

Targeted

SMi Trial Results

  •    Reduce deviation rates
  •    Save hundreds of thousands
            of dollars in downstream monitoring
  •    Lower overall subject costs
  •    Expedite time-to-market

SMi Trial Results

  •    Reduce deviation rates
  •    Save hundreds of thousands
             of dollars in downstream monitoring
  •    Lower overall subject costs
  •    Expedite time-to-market

Get in touch with us

Complete the form below and click on the button 'Request Demo'.

We'll get back to you in 1-2 business days.