Medvice Consulting, Inc.
Regulatory and quality consulting practice led by experienced nurse-executive consultants. Services focus on regulatory compliance and accreditation readiness (including contagious disease/infection prevention), risk assessment, corrective action planning, data-driven quality improvement, and real-time support during regulatory inspections. Operates remotely and is licensed to consult in multiple U.S. states.
Industries
N/A
Nr. of Employees
small (1-50)
Medvice Consulting, Inc.
Products
Healthcare Consulting Services
Consulting services specializing in regulatory compliance, mock surveys, CMS compliance, survey readiness, and corrective action planning for healthcare organizations.
Healthcare Consulting Services
Consulting services specializing in regulatory compliance, mock surveys, CMS compliance, survey readiness, and corrective action planning for healthcare organizations.
Services
Mock surveys, gap analysis reports cross-referenced to standards, manager and frontline staff preparation, and standardized policy/procedure development for accreditation readiness.
Rapid deployment to facilities during regulatory visits to interpret findings, liaise with surveyors, and support organizational responses.
Design of plans of correction, establishment of tracking processes, scheduled remote meetings for accountability, and status reporting to leadership.
Design and implementation of QAPI programs, metric selection, methodology for core/quality measures tracking, and facilitation of data-driven performance projects.
Construction of dashboards and single-page indicator views, metric aggregation from multiple sources, and reporting tools to support leadership and frontline staff.
Assessment and construction of infection prevention programs, sterile processing guidance, and integration with accreditation and quality processes.
Mock surveys, gap analysis reports cross-referenced to standards, manager and frontline staff preparation, and standardized policy/procedure development for accreditation readiness.
Rapid deployment to facilities during regulatory visits to interpret findings, liaise with surveyors, and support organizational responses.
Design of plans of correction, establishment of tracking processes, scheduled remote meetings for accountability, and status reporting to leadership.
Design and implementation of QAPI programs, metric selection, methodology for core/quality measures tracking, and facilitation of data-driven performance projects.
Construction of dashboards and single-page indicator views, metric aggregation from multiple sources, and reporting tools to support leadership and frontline staff.
Assessment and construction of infection prevention programs, sterile processing guidance, and integration with accreditation and quality processes.
Expertise Areas
- Regulatory compliance and accreditation
- Infection prevention and control
- Quality assurance and performance improvement (QAPI)
- Risk management and immediate regulatory response
Key Technologies
- Electronic health record (EHR) systems
- Electronic event/incident reporting systems
- Data visualization and business intelligence tools
- Spreadsheets and relational data tools
News & Updates
Prepared and led over 50 regulatory visits; reported results of full accreditation outcomes and zero FDA observations in referenced engagements.
Hosted more than 30 FDA visits in Missouri and Arkansas without FDA observations while overseeing regional quality.
Prepared and led over 50 regulatory visits; reported results of full accreditation outcomes and zero FDA observations in referenced engagements.
Hosted more than 30 FDA visits in Missouri and Arkansas without FDA observations while overseeing regional quality.