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DDOTS

by DDOTS
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Quick facts
VendorDDOTS
Year launchedN/A
StatusActive
LocationN/A
Countries servedN/A
Languages1
IntegrationsN/A
Free tierNO
Free trialNO
Contact salesYES

About DDOTS

DDOTS provides a suite of integrated software solutions for modern research.

DDOTS offers a comprehensive platform of software solutions designed for the needs of modern research organizations. The company provides several interconnected modules, including a Clinical Trial Management System (CTMS), Pharmacy management for investigational drugs, a Biorepository for sample management, and an Institutional Review Board (IRB) module. A key feature is the integrated eRegulatory functionality, which is embedded across all solutions to handle electronic documents and Part 11-compliant e-signatures, streamlining compliance and reducing administrative overhead. The platform is designed for seamless integration with existing systems like EHRs via HL7 and supports Single Sign-On. DDOTS emphasizes its nearly 30 years of experience in the field. The website does not provide public pricing, requiring potential customers to contact them for a quote. Support is offered via a direct contact person and online tools.

Pros & Cons

Pros
  • Offers a single, integrated platform with multiple solutions for research management (CTMS, Pharmacy, Biorepository, IRB).
  • Includes built-in eRegulatory features with Part 11-compliant electronic signatures.
  • Supports integration with EHRs via HL7 and offers an API for other system connections.
  • The company has nearly 30 years of experience developing research software.
Cons
  • Pricing is not publicly available and requires contacting the company.
  • No free trial or free tier is mentioned on the website.

Features

Key features

Clinical Trial Management (CTMS)

Centralizes management of study start-up, enrollments, compliance, financials, and reporting.

Pharmacy Management

Manages investigational drugs, including accountability, compliance, and customizable electronic Drug Accountability Record Forms (DARFs).

Biorepository Management

Manages biological samples alongside clinical trial data, tracking location, consent, and chain of custody.

IRB Management

Unifies clinical trial and IRB submission management to simplify workflows and enhance study oversight.

Integrated eRegulatory

Provides secure, centralized document storage and Part 11-compliant electronic signatures across all solutions.

System Integration

Offers interfaces with EHRs using HL7, an API for connecting with other departments, and Single Sign-On (SSO) support.

Configurability

Allows for customization of system behavior and data management to fit specific research needs.

Reporting

Includes over 100 standard reports for protocols, participants, regulatory, and financials, with options for custom report development.

Pricing

Free trial
Free version
Request a quote
Promo Offer

Countries & Languages

Countries served
1
Interface languages
Billing currencies

Interface languages

English

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