i-CDMS by Infoset

i-CDMS software reviews, alternatives, pricing, & feature 2026

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Clinical Trial Management Software

i-CDMS reviews and summary

i-CDMS, by Infoset, is an electronic data capture (EDC) and electronic case report form (eCRF) system promoted as the investigator's first choice for managing data in clinical trials. It is designed to streamline the process of collecting, validating, and managing clinical trial data electronically, replacing cumbersome paper-based methods. The system likely offers features such as form design, data validation checks, query management, and reporting tools to ensure data accuracy, integrity, and regulatory compliance across various trial phases and types. This EDC system is intended for clinical investigators, research site coordinators, and sponsors conducting a wide range of clinical trials, from early-phase studies to large-scale multi-center trial...

Best for

This EDC system is intended for clinical investigators, research site coordinators, and sponsors conducting a wide range of clinical trials, from early-phase studies to large-scale multi-center trials. It is particularly aimed at those seeking a user-friendly, reliable, and efficient electronic solution to capture and manage patient data directly from the source.

Vendor Infoset
Key takeaways

Our verdict

i-CDMS positions itself as a user-centric EDC solution, potentially offering simplicity and reliability that appeals to investigators at the site level. If it delivers on its promise of being the 'first choice,' it could be a strong contender in the EDC market by reducing the data capture burden and improving data quality for clinical research teams.

Quick facts

i-CDMS at a glance

Vendor Infoset
Ratings

i-CDMS ratings

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Decision notes

i-CDMS pros and cons

Potential strengths

  • Clear buyer-fit positioning is available in the profile data.

Points to verify

  • Confirm current pricing, contract terms, and included plan details with the vendor.
  • Confirm product-specific availability for category-level features before buying.
  • There are no written reviews for this software yet.
  • Published pricing is not available in this profile data.
Buyer fit

Who uses i-CDMS?

This EDC system is intended for clinical investigators, research site coordinators, and sponsors conducting a wide range of clinical trials, from early-phase studies to large-scale multi-center trials. It is particularly aimed at those seeking a user-friendly, reliable, and efficient electronic solution to capture and manage patient data directly from the source.

Feature research

i-CDMS features

These are common features buyers compare in Clinical Trial Management Software. Product-specific availability should be confirmed with the vendor.

21 CFR Part 11 Compliance

Helps buyers evaluate how access, control, and evidence are handled for sensitive or regulated work.

Data Import/Export

Shows how well the product can connect with existing systems and reduce duplicate data entry.

Document Management

Keeps important files and records close to the workflow, with easier search, review, and handoff between teams.

Double Data Entry

Helps buyers judge whether double data entry fits the way their team handles clinical trial management work.

Electronic Data Capture

Helps buyers judge whether electronic data capture fits the way their team handles clinical trial management work.

EMR/EHR

Helps buyers judge whether EMR or EHR fits the way their team handles clinical trial management work.

Financial Management

Connects money-related work with the rest of the clinical trial management process so charges, approvals, and records are easier to review.

HIPAA Compliant

Helps buyers judge whether HIPAA compliant fits the way their team handles clinical trial management work.

Inventory Management

Tracks the items, locations, or resources the team depends on so availability and ownership are easier to confirm.

Patient Management

Keeps person or account details tied to the work they affect, instead of leaving context scattered across notes and inboxes.

Patient Monitoring

Gives managers a clearer view of activity, exceptions, and trends so they can spot issues before they turn into rework.

Patient Recruiting

Keeps person or account details tied to the work they affect, instead of leaving context scattered across notes and inboxes.

Compare

i-CDMS alternatives

Compare i-CDMS with other Clinical Trial Management Software tools that buyers often evaluate.

Castor EDC by Castor

4.7 (124)

Castor EDC is an electronic data capture platform for clinical trials that helps research teams build studies, integrate data from multiple sources, and run decentralized trials wi...

RealTime-CTMS by RealTime-CTMS

4.9 (62)

RealTime-CTMS is a clinical trial management system developed to streamline and optimize operations at research sites and site networks. It provides a centralized platform for mana...

Medrio by Medrio

4.6 (51)

Medrio is an eClinical software suite known for its speed and ease of use, offering electronic data capture (EDC) and other clinical trial solutions. A key advantage is that it req...

Research Manager by Cloud9-Software

4 (42)

Research Manager is an online research platform that facilitates everything related to life sciences research and registrations. It acts as a central hub where researchers, researc...

Ripple by Ripple Science

4.8 (32)

Ripple, developed by Ripple Science, is a specialized software platform designed to facilitate patient recruitment and management for clinical and translational research studies. I...

Clinical Conductor CTMS by Advarra

4.6 (30)

Clinical Conductor CTMS, offered by Advarra, is positioned as a leading clinical trial management system specifically tailored for the operational needs of research sites. It provi...

EDGE by CIRU, University of Southampton

4.9 (28)

EDGE is an innovative, cloud-based clinical trial management system developed by the University of Southampton's CIRU. It is a global platform designed to accelerate clinical resea...

TrialKit by Crucial Data Solutions

4.5 (28)

TrialKit is a flexible clinical trial technology platform that empowers all users to collect, access, and manage study data from any location. It provides robust electronic data ca...

Software reviews

i-CDMS software reviews

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FAQ

i-CDMS FAQs

i-CDMS, by Infoset, is an electronic data capture (EDC) and electronic case report form (eCRF) system promoted as the investigator's first choice for managing data in clinical trials. It is designed to streamline the process of collecting, validating, and managing clinical trial data electronically, replacing cumbersome paper-based methods. The system likely offers features such as form design, data validation checks, query management, and reporting tools to ensure data accuracy, integrity, and regulatory compliance across various trial phases and types.

This EDC system is intended for clinical investigators, research site coordinators, and sponsors conducting a wide range of clinical trials, from early-phase studies to large-scale multi-center trials. It is particularly aimed at those seeking a user-friendly, reliable, and efficient electronic solution to capture and manage patient data directly from the source.

i-CDMS is listed in Clinical Trial Management Software.

i-CDMS is listed with Infoset as the vendor.

Buyers often compare i-CDMS with other Clinical Trial Management Software tools such as Castor EDC, RealTime-CTMS, Medrio, Research Manager. Review ratings, pricing, and fit before choosing.

Yes. Use the Write a review button on this page to submit a software review for i-CDMS.
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