thinkClinical is an innovative Clinical Data Collection & Management software solution package, whose unified platform includes EDC and eDiary with randomization and trial supply management.  Trials are completely configurable without any programming through the web interface.  The system includes a drag and drop designer for CRFs and diary screens with an advanced rules engine to configure dynamics, edit checks, and notifications.  CRFs and diary screens with configured rules can easily be re-used across trials, resulting in faster study startup and promoting consistent design standards.  

All capabilities in the system including randomization, supply management, and laboratory normal ranges are also configurable through the same interface.  The data management workflow is also configurable in the system to meet the needs of each individual trial from phase I to post marketing and surveillance trials.  Test data can be entered during the trial design, providing the ability for designers to immediately verify their work.

Focus on the Trial, Not the Technology

unithink is more than just a technology vendor.  unithink is an eClinical service provider whose employees have years of experience in clinical trials.  The configurable design in thinkClinical allows unithink to provide a team with the necessary clinical trials experience so the CRFs in the system can be created directly from the protocol instead of requiring detailed specifications from the client.  The result is reduced chances of study updates due to incomplete or improper CRF design as well as faster design and reduced client workloads.

Adaptive workflows

Trials are often managed differently across companies and stages in the clinical trials process.  A phase I trial at one company will be run much differently than a post marketing or surveillance trial at another.  Many systems offer a very rigid set of features to manage the data review process, dictating instead of supporting the client's workflow. This can require additional work and increase the potential for error as sponsors and CROs change their processes to fit the capabilities of a system.