Investigator Inquiry

DRC, LLC will provide access to new clinical trials every Month as well as complete management of the Startup Process up to SIV.

DRC, LLC will handle the Contract & Budget Review for all New Clinical Trials

DRC, LLC will negotiate the budget with sponsor to cover all study related site cost.

DRC, LLC offers Study Startup and Visit completion invoicing on all projects.

Tracking and documenting completion of all study related visits to assess earned revenue and then invoicing the sponsors monthly to ensure that all funds are received at your site timely and correctly. 

Generally all patients will be paid a stipend for their participation. DRC, LLC will issue each patient a debit card loaded with the funds that is owed to them. DRC,LLC will prepare the account, issue the debit card and load the debit card per completed visit for the patient.

DRC, LLC will prepare and submit the required annual report to the IRB, updating them about your study progress. 

DRC, LLC will audit your site to make sure that all clinical trials are being processed correctly and all documents are in order.

If the sponsor wants to come audit your site, DRC, LLC will review your study to make sure that all aspects of the clinical trial are in order.

If your contract ever needs to be amended, DRC,LLC will take care of the negotiations.   DRC, LLC performs an internal analysis to determine all study related costs, then negotiates directly with the study sponsor for the support that is needed.

DRC, LLC will take care of packaging, labeling and shipping of all study related documents for your practice. 

DRC, LLC will provide a research study coordinator at your site to manage the required clinical trial visits.  If you have a potential coordinator at your site already, DRC, LLC will train any of your nurses to be a study coordinator.

Once the study is over, the sponsor will need to conduct a closeout visit. DRC, LLC will look over your study documents and make certain that all documentation is complete, in preparation for the closure of the study.

DRC, LLC will assist in the development of your research department at your site.  DRC, LLC will meet with you and determine the types of trials that your research department would like to conduct and assist in the preparation of your department to accept the clinical trial.

DRC, LLC will walk your site through the Site Qualification Visit in order to provide support in obtaining your first clinical trial.

For completed Trials

For all active Trials

For appropriate coverage of study costs

Review current Clinical Trials Management System and make suggestions for improvements

 Research related

* Make suggestions for CTA standard verbiage (Master Agreement) and standardize fixed costs pertaining to the study budget.

 Clinical Trial Lifecycle workflow

Working Instructions Manual for staff