Introducing CTrials by BRANY

Accelerates study pipelines.
CTrials promotes investigators and sites to our network of established CRO’s, pharmaceutical, biotech and device companies, and provides immediate access to those relationships. CTrials is constantly matching investigators and site profiles in our database to sponsor/CRO studies so there are always new, and relevant, trial opportunities. And to alleviate your administrative burden, we take care of the CDA process and sponsor coordination.

Optimizes trial revenue and cash flow.
CTrials makes a tangible contribution to the financial health of the study. The CTrials team’s experience and expertise in research study financials ensures that:

• Accurate clinical trial budgets identify hidden costs and administrative fees
• Expert coverage analysis and billing grids provide clear guidance for insurance and sponsor-covered procedures
• Budget negotiations that maximize trial budget and overhead allocation
• Study revenue collection is maximized through efficient research billing and collections

Provides structure and streamlines processes.
For hospitals and institutions with minimal structure, CTrials provides the administrative structure and transparent communications set up that is necessary to ensure clinical trial success. CTrials is run by a team of research administration experts that connects the trial identification with rapid study start up all the way to the billing and collection process. You can also turn to BRANY for your IRB reviews.

Avoid costs with temporary staff augmentation.
CTrials can augment staff where it is needed most, providing an opportunity to fill in short-term gaps for costs savings while the research infrastructure is ramping up.

Alleviates administrative burden.
CTrials lets research teams focus on the tasks that are critical to the success of the trial, such as subject enrollment and completing trial procedures. CTrials’ team professionally handles all the administrative tasks that can bog down research teams like:

• Completing regulatory startup documents, including Informed Consent forms
• Performing coverage analysis and developing accurate billing grids
• Negotiating budget line items and contract terms
• Invoicing sponsors and collecting revenue in a timely fashion

Protects sites and human subjects.
CTrials’ team of experts ensure that clinical trial agreements include rigorous terms. This encompasses indemnifications, insurance provisions that are suitable to cover potential claims, and clear stipulations to address subject injury, protect intellectual property, while meeting AAHRPP standards.

Complimentary access to our SMART CTMS.
All of our trials are coordinated through our SMART CTMS. This provides you with immediate access to a clinical trial management system without incurring expensive licensing or set up costs.