REGULATORY DOCUMENT
MANAGEMENT FROM VACAVA

Redefine your clinical trial regulatory document management process with an online easy-to-use, customizable VACAVA solution. CROs, SMOs, sponsors and sites can now manage regulatory documents and signatures electronically, securely, anywhere, anytime.

READ THE ACRP CLINICAL RESEARCHER ARTICLE

Regulatory Management Solutions

Healthcare solutions from VACAVA reduce the complexity and cost of clinical trial regulatory document management. Each time documents move through a manual workflow, it introduces the opportunity for delays and lost information. VACAVA solutions help you streamline regulatory processes by storing profiles, forms and documents in a single easy-to-access online location. Documents seamlessly move through your workflow with approvals captured electronically (21 CFR Part 11 compliant). Easy-to-read dashboards enable efficient management.

VACAVA’s Regulatory Document Management System was built in collaboration with a major clinical trial research base to simplify operations and radically increase efficiency. VACAVA’s Regulatory Document Management System is surprisingly affordable and can be customized to meet your unique needs. VACAVA’s solutions are flexible, scalable, and delivered via the cloud so you never have to worry about managing servers, security, and backups. VACAVA handles all that for you.

Benefits

SIMPLIFIED TRIAL & DOCUMENT MANAGEMENT
DOCUMENT ACCESS ANYWHERE, ANYTIME
SECURE DOCUMENT SHARING
DYNAMIC DATA UPDATES
MANAGED COMPLIANCE
CUSTOMIZABLE

Features

TRIAL & DOCUMENT MANAGEMENT DASHBOARDS
ELECTRONIC SIGNATURE CAPTURE
AUTOMATIC FORM POPULATION
DEADLINE TRIGGERS
CHANGE HISTORY
SCALABLE

Case Studies

Clinical Trial Regulatory Document Management

A leading cancer center recognizes an opportunity to dramatically reduce the complexity and cost of clinical trial regulatory document management.

See How

A Case Study in Redefining Regulatory Binder Management

Paperless regulatory document management is a hot topic as clinical researchers strive to increase productivity, speed study start-up, and improve inspection readiness. The Association of Clinical Research Professionals, ACRP, Clinical Researcher published a case study of innovation and transformation that is demonstrating quantifiable benefits via VACAVA's regulatory document management solution.

See How

SEE A LIVE DEMO

Name*
Email*
Phone*
Message*
Comments

This field is for validation purposes and should be left unchanged.
Best time to contact you?

507-252-9076

REGULATORY DOCUMENT MANAGEMENT FROM VACAVA