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Medical Device Train the Trainer Summit Event Recap Engaging Learners | Leveraging Tactile Experiential Education | Effective Course Evaluation By Kate Jeter, Director at Q1 Productions Attending the Annual Q1 Medical Device Train the Trainer Summit is always a...

Most Common Symbols and What They Mean

Clarification of Regulatory Requirements for Companion Diagnostics & NGS, Insight into the Status of Laboratory Developed Test Specific Policies, all while Strategizing to Ensure Compliance with New European & Asian Market Rules
DECEMBER 5-6, 2018 | ALEXANDRIA, VA | EMBASSY SUITES BY HILTON ALEXANDRIA OLD TOWN

Analyses of Shifting Healthcare Market Dynamic to Optimize Diagnostic Reimbursement Strategies | Focus on Trends Impacting the Industry such as Value-Based Agreements & Increasing Prior Authorization | Deciphering Public & Private Payer Cost-Efficiency Requirements & LBMs’ Involvement
DECEMBER 6-7, 2018 | BOSTON, MA | HILTON BACK BAY

Employing Continuous and Stringent Postmarket Product Monitoring through Thorough Complaint and Feedback Intake Strategies, Streamlining Escalation Operations and Utilization of Compliant Reporting Methodologies to Ensure Long Term Medical Product Safety and Quality
JANUARY 30-31, 2019 | ALEXANDRIA, VA

Analyses of Shifting Healthcare Market Dynamic to Optimize Diagnostic Reimbursement Strategies | Focus on Trends Impacting the Industry such as Value-Based Agreements & Increasing Prior Authorization | Deciphering Public & Private Payer Cost-Efficiency Requirements & LBMs’ Involvement
FEBRUARY 12-13, 2019 | SAN DIEGO, CA

Development & Execution of Innovative & Engaging Sales Training & Education Platforms that Elevate Skills to Meet the Rising Demand of a Value-Based Selling Environment through the Leverage of Resources, Technology & Tools which Support Training while Analyzing Metrics that Drive Forward Return on Investment
FEBRUARY 26-27, 2019 | CHARLOTTE, NC

Defining the Primary Mode of Action as a Drug or Device to Determine FDA Jurisdiction, Ensuring Optimized Human Factors Study Design to Prove Safe Patient Use, while Maintaining Compliance With Post Market Reporting Requirements
FEBRUARY 28 – MARCH 1, 2019 | ARLINGTON, VA