Paper consent forms?

With our controlled workflow make the whole consenting process completely paperless and transparent.

Unethical subject recruitment?

Prevent duplication of cases and false data entry through biometric verification of your subjects during consenting.

Poor adherence to study protocol?

CliniSite can automatically alert patients for visit & dose regimen.

Want more patient involvement?

Your subjects can now login to our web portal using secured login system to view their personal data.

Want to empower your patients?

Instead of going to a site location for a scheduled visit, patient can upload their self-report data remotely.

Want to engage your patients?

Engage your patients by giving them access to custom designed interactive games & useful study related data.

CliniPatient

CliniPatient enables you to keep your patients engaged, involved, and interested in the study they are participating in thereby improving response to self reported data, decreasing mid-study drop-offs and improving adherence to protocol.

Paper consent forms?

– Now a thing of the past

Your participants can now sign the consent forms electronically. Our controlled workflow provides checks and balances to ensure that the consent form is signed before any data is collected making the whole consenting process completely paperless and transparent.

Document IT
Document IT

Unethical subject recruitment?

– Enable Biometric Patient enrollment

Prevent duplication of cases and false data entry through biometric verification of your subjects during consenting. Subjects can even choose to sign their consent forms using their fingerprint.

Poor adherence to study protocol?

– Alert patient for visit & dose regimen

CliniSite can automatically send alerts and notifications to your subjects to remind them to take medicine or follow directions from previous visits and also notify them about their upcoming visits so they don’t miss any of their scheduled visits.

Document IT
Document IT

Want more patient involvement?

– Leverage our subject portal features

Your subjects can now login to our web portal using secured login system to view their personal data, and keep a track of all upcoming visits. Here patients can also approve their records.

Want to empower your patients?

– Enable remote self-report data entry

Instead of going to a site location for a scheduled visit, patient can upload their self-report data remotely. This not only saves time and money for the patient but also improves response rates.

Document IT
Document IT

Want to engage your patients?

– Engage subjects with interactive gamification

Engage your patients by giving them access to custom designed interactive games and also by providing them with useful study related data for educational purposes.

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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