Digitize source and regulatory documents

Broadneck offers a proprietary and revolutionary platform for information management in clinical trials. At Broadneck, we also provide consulting services to help clinical trial operators manage their information with superior results. 

Streamline operational workflow

Our calendar-centric software simplifies study management with intuitive features and powerful automations. By reducing administrative burdens, study teams can focus on patient care while staying seamlessly connected from any location.

SCALE Quickly

Securely manage users to make a fast onboarding process feel effortless. 

All source documents were easy to locate and simply a click away. In my opinion, this is a CRA’s dream because it allows for a quicker and more efficient source data review/verification. Also, with everything being electronically uploaded, I will be able to monitor at the comfort of my own home in the near future. Thank you MD Medical Research, for giving me the right tools to be able to be a productive CRA.

Security

​Protect patient data with HIPAA-compliant encryption and protocol-specific safeguards.

Compliance

Stay aligned with FDA, GDPR, ALCOA, and GCP standards at every stage of your trial.

Governance

Control access at the delegation level and customize permissions to meet each study’s unique requirements.