Takes months for study setup?

We give you unprecedented speed and agility.

Problems keeping studies on track

Our rich reporting capabilities will lead to improved decision making with near-real time updates from your sites.

Worried about mid-study changes?

Seamlessly introduce mid-study changes without spending weeks on database lock, data migration and site coordination.

No internet?

CliniTrial Lite makes data collection using mobile devices easy, quick, and accurate with a user friendly interface, instant edit checks, photo/video upload capabilities etc.

Tired of data transcription?

Reduce your data collection time and increase your data quality by utilizing our integration features.

Data standardization across studies

Use eCRFs from our CDASH compliant library to generate CDISC-compliant SDTM datasets.

Worried about compliance?

CliniTrial is compliant with 21 CFR Part 11 and HIPAA. It provides key clinical data integrity and security features.

Problems tracking site performance?

With our site level dashboard get a quick overview of your site performance and also compare your site metrics with other sites, in the study.

Want to leverage our eSource solution?

Our tablet based eSource solution, can be seamlessly integrated with other eClinical tools to offer you all the benefits.

CliniTrial

CliniTrial offers you the flexibility of setting up and analyzing your study on our web-based application, while capturing data offline at source, using our tablet-based application ‘CliniTrial Lite’. Thus CliniTrial provides a host of innovative features such as Intelligent edit checks, workflow based design and integration capabilities that will automate and streamline your data collection process into an efficient system and make information available for reporting and analysis in near real-time.

Takes months for study setup?

– We give you unprecedented speed and agility

Our intuitive point & click interface with extensive form libraries, variables, dynamic form rules and custom skip logic will not only help in having consistent configuration across multiple studies but will also help in post-study data management.

Document IT
Document IT

Problems keeping studies on track

– Rely on our reporting system

Improved decision making with near-real time updates from your sites. Our rich reporting capabilities will empower you to prepare your reports with near real-time data to analyze trends, find discrepancies, monitor site compliance, and identify underperforming sites to ensure that your trials stay on track.

Worried about mid-study changes?

– We offer flexibility and streamlined workflow

Seamlessly introduce mid-study changes without spending weeks on database lock, data migration and site coordination. Leverage CliniTrial to update the study requirements via the portal and send your updated study configuration with push notification.

Document IT
Document IT

No internet?

– Collect your data offline

Capture data offline using a tablet and sync online. CliniTrial Lite makes data collection using mobile devices easy, quick, and accurate with a user friendly interface, instant edit checks, photo/video upload capabilities etc. With CliniTrial Lite, you can access the site data without the need for internet connection.

Tired of data transcription?

– Integration is the solution

Reduce your data collection time and increase your data quality by utilizing our integration features. CliniTrial Lite integrates with various medical devices and software to automate and streamline the data collection procedure and significantly cut down on verification costs.

Document IT
Document IT

Data standardization across studies

– Leverage CDISC compliant solution

Use eCRFs from our CDASH compliant library to generate CDISC-compliant SDTM datasets. Your eCRF design time will be shortened as CDASH eCRF forms can be pulled out of our library. FDA recommends CDISC data standards, and will in the near future require all submissions to be CDISC-compliant.

Worried about compliance?

– We have the solution

CliniTrial is compliant with 21 CFR Part 11 and HIPAA. It provides key clinical data integrity and security features including audit trails, time stamps, date stamps, and encryption.

Document IT
Document IT

Problems tracking site performance?

– Use our site analytics

With our site level dashboard get a quick overview of your site performance and also compare your site metrics with other sites, in the study. All our metrics are based on SMART attributes (Simple, Measurable, Actionable, Real, Timely) so sites can focus on KPI that matters.

Want to leverage our eSource solution?

– CliniTrial Lite gives you all the benefits

Our tablet based eSource solution, can be seamlessly integrated with other eClinical tools to offer you the benefits of offline data capture, medical device integration, multi-lingual support and various other benefits and enable you to streamline your data sourcing, data management and reporting requirements.

Document IT

Project
Management

Our experienced Project Managers can plan, organize, motivate and control your resources to achieve your specific goal(s).

Quality
Management

For more than 15 years Document IT & its partners have been at the forefront of computerized system validation & IT system compliance.

Quality Management

Business
Consulting

Our consultants work with clients to model & improve business processes, streamline operations & assure compliance.

Business Consulting

Resourcing
Services

Our resourcing services are open to any industry looking for a highly skilled worker.

Outsourcing

We currently offer full business process outsourcing within our CDISC Factory for clinical business processes around the usage of standardized clinical data.

Outsourcing

Bio Statistics

Our expertise includes the design & conduct of clinical experiments, the method & way in which data is collected, analysis of data & interpretation of results.

Clinical
Programming

We offer you comprehensive range of high-quality & cost-effective clinical programming services.

Clinical Programming

Clinical Data
Management

We provide end to end clinical data management solutions from data management plan to database lock.

Clinical Data Management

CDISC
Factory

Document IT’s CDISC factory supports & accelerates the set-up of CDISC compliant systems & conversions of legacy clinical trial data to the CDISC standards.

Records
Management

Document IT maintains the records & documents throughout their life cycle from the time they are created until their disposal.

Records Management
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