Compliance
An audit-ready structure designed to support ICH-GCP and 21 CFR Part 11 requirements.
Products · Clinical Research
Manage clinical research with confidence.
NarCRO brings clinical research workflows, patient and study management, data collection, and regulatory compliance together on one platform.
- ICH-GCP support
- eCRF & data entry
- Patient tracking
- Audit trail
NarCRO
50%faster data entry
100%data traceability
40% lowercompliance risk
21 CFRPart 11 support
Overview
What is NarCRO?
One platform for managing clinical study data and workflows.
NarCRO digitizes every stage of clinical research, from study planning and data collection to patient tracking and audits. Electronic data capture (eCRF) records information directly, with validation and traceability.
Designed with regulatory compliance (ICH-GCP, 21 CFR Part 11) in mind, the platform provides an audit trail, data validation, and role-based access for a reliable research environment.
Why NarCRO
Why NarCRO?
Data quality
Improve data quality with validation rules and double-entry checks.
Speed
Reduce study timelines with electronic data capture.
Visibility
Monitor study status, records, and deviations in real time.
Modules
NarCRO modules
Modules that support every stage of clinical research.
Study Management
Manage protocols, sites, and study teams in one place.
eCRF & Data Entry
Collect validated data through electronic case report forms.
Patient Tracking
Monitor enrollment, visits, and eligibility workflows.
Visit Planning
Manage visit schedules and automated reminders.
Quality & Monitoring
Support source verification and deviation management.
Reporting
Generate study reports and audit outputs.
Process
How do we implement it?
A tailored setup and compliance process for your study.
-
01
Discovery & Analysis
We review your protocol and study requirements.
-
02
Setup & Configuration
We build your eCRF forms and study structure.
-
03
Compliance & Validation
We configure regulatory support and data validation rules.
-
04
Launch & Support
We launch the study, train your teams, and provide ongoing support.
50%
faster data entry
100%
data traceability
40% lower
compliance risk
21 CFR
Part 11 support
Integrations
Integrations
Connect with systems across your research ecosystem.
Use cases
Clinical research centers
Pharmaceutical companies
CROs
University hospitals
Research institutes
Biotechnology
Healthcare organizations
R&D teams
FAQ
Frequently asked questions
Does NarCRO support regulatory requirements?
Yes. It is designed around ICH-GCP and 21 CFR Part 11 requirements and maintains an audit trail.
Can eCRF forms be customized?
Yes. You can define study-specific eCRF forms, validation rules, and visit schedules.
Are multi-site studies supported?
Yes. Multi-site and international studies can be managed with role-based access.
How is data security handled?
Encryption, audit trails, backups, and role-based access help protect data integrity.
How long does implementation take?
Typical implementation takes 3–8 weeks, depending on study scope.
Digitize your clinical study.
Tell us about your study requirements and we’ll plan a tailored solution.
