Home / Clinical Technologies /

Almac Visit Management:

Smarter scheduling for modern trials
Almac’s Visit Management solution, part of the Almac Trial Coordinator™ ecosystem, empowers sponsors and sites to deliver efficient, compliant, and participant-friendly visit scheduling purpose-built for the demands of modern clinical trials.

Download Factsheet
woman using Almac Visit Managemnet on computer

Visit Management Key Features

Automated Scheduling Icon

Automated Scheduling

Enforces protocol compliance, reduces administrative burden, and minimises missed visits.
Flexible Visit Types Icon

Flexible Visit Types

Supports on-site, remote, hybrid, and home-based visits for maximum adaptability.
Real-Time Oversight Icon

Real-Time Oversight

Live dashboards for sponsors and sites, with compliance tracking and instant visibility into study progress.
Participant-Centric Design Icon

Participant-Centric Design

Multilingual, accessible, and offline-capable app with smart reminders and progress views.
Compliance & Security Icon

Compliance & Security

GxP validated, GDPR and HIPAA compliant, 21 CFR Part 11 audit trail, ISO 27001 certified, and backed by Almac’s global Quality Management.

Why choose Almac Visit Management?

Protocol Adaptive Scheduling
Protocol Adaptive Scheduling: Automate visit planning based on protocol parameters. Assign rooms, staff, and visit windows to reduce deviations and ensure compliance.
Participant-First Design
Multi Study Coordination & Resource Management: Centralise scheduling across studies and sites. Optimise appointment slots and allocation of rooms, staff, and equipment.
Expert Service & Support
Participant Engagement: Improve retention with a user-friendly app offering reminders, preparation guidance, and support for on site, homecare, phone, or tele visits.
Global Reach & Reliability
Integrated Communications: Streamline confirmations, reminders, and support through automated messaging to keep participants informed and prepared.

Proven Global Delivery

Achieved 98.3% protocol adherence in global oncology trials

Enabled a 42% reduction in missed visits in high-complexity studies

100+
trials supported
25+
countries
250+
sites

How It Works

1
Protocol-Driven Scheduling: Automates visit planning and resource assignment.
2
Participant App: Delivers reminders, visit details, and support for all visit types.
3
Centralised Management: Sites and sponsors coordinate multi-study operations from a unified dashboard.
4
Integrated Communications: Automated emails and notifications keep participants informed.

 

  • Uniting trial workflows
  • Guiding study teams
  • Retaining participants
Learn more
This website uses cookies. By continuing to browse the site, you are agreeing to our use of cookies