Late Phase Trials

eLearning – Clinical Trial Training Management

The eLearning module is a centralised clinical trial training solution designed to standardise, deliver, and document protocol and role-based training for all study personnel. It ensures that investigators, site staff, and study teams are adequately trained and certified before performing study activities, while maintaining complete, verifiable evidence to support audits, inspections, and regulatory compliance. By enabling structured training delivery, automated certification, and full training traceability, the eLearning module reduces operational risk, supports consistent study execution, and strengthens overall trial quality across global studies.

Key Benefits

1

Training Consistency

Ensures uniform protocol understanding across all sites and users.

2

Regulatory Compliance

Provides documented evidence of GCP and protocol training compliance.

3

Audit Readiness

Enables complete, traceable training documentation for inspections.

4

Risk Reduction

Reduces protocol deviations caused by insufficient or outdated training.

5

Operational Efficiency

Streamlines training management and accelerates site readiness.

6

Certified Competency

Ensures study activities are performed only by trained and certified personnel.

Key Functionalities

Protocol Training
Delivers standardised, study-specific protocol training to trial personnel.
Role-Based Learning
Assigns training modules based on defined roles and responsibilities.
Content Management
Manages training content, versions, and updates aligned with protocol amendments.
Assessment Testing
Validates learner understanding through configurable assessments and quizzes.
Certification Generation
Automatically issues training certificates upon successful completion.
Training Tracking
Tracks training status, completion dates, and re-training requirements in real time.
Audit Evidence
Maintains time-stamped, inspection-ready records of all training activities.
Access Control
Ensures secure, role-based access to training content and records.
00%

faster study start-up through streamlined protocol training

00%

reduction in training-related protocol deviations

00%

decrease in audit findings related to training documentation

00%

traceable, time-stamped training and certification records

Let's understand how you manage your Late Phase Studies?