BSI CTMS

For the management of clinical studies.

Visit Website →

Overview

BSI CTMS is a clinical trial management system that helps sponsors, CROs, and research institutions manage their clinical studies. It supports study planning, site and patient management, monitoring, and document tracking. The system is designed to be flexible and can be adapted to various study types and organizational workflows.

✨ Key Features

  • Study Planning & Management
  • Site & Contact Management
  • Subject Tracking & Management
  • Monitoring & Visit Reports
  • Document Management
  • Integration with EDC and eTMF

🎯 Key Differentiators

  • Flexibility and configurability.
  • Strong presence in the European academic research market.
  • Part of a broader suite of BSI eClinical solutions.

Unique Value: Offers a highly flexible and configurable CTMS that can be tailored to the specific processes of different research organizations, supported by a suite of integrated eClinical tools.

🎯 Use Cases (3)

Managing academic or commercial clinical trials. Centralizing study information for sponsors and CROs. Tracking site performance and monitoring activities.

✅ Best For

  • European-based clinical trials and academic research.

💡 Check With Vendor

Verify these considerations match your specific requirements:

  • Organizations looking for a very simple, out-of-the-box solution with minimal configuration.

🏆 Alternatives

Veeva Vault CTMS Medidata Rave CTMS

Provides more customization options than some of the larger, more rigid SaaS platforms.

💻 Platforms

Web

🔌 Integrations

BSI eTMF BSI EDC BSI Randomization

🛟 Support Options

  • ✓ Email Support
  • ✓ Phone Support
  • ✓ Dedicated Support (All tier)

🔒 Compliance & Security

✓ HIPAA ✓ BAA Available ✓ GDPR ✓ ISO 27001 ✓ SSO ✓ GCP ✓ ISO 9001

💰 Pricing

Contact for pricing
Visit BSI CTMS Website →