Events

Conferences

8TH ANNUAL EU MEDICAL DEVICE REGULATORY AFFAIRS CONFERENCE

Clarifying the Notified Body Redesignation Status & Product Recertification Capacity by 2020 Comprehensive Prioritization of Tasks to Optimize the Remaining Transition Time Ensuring Pragmatic Legacy Device Business Decisions as well as & QMS Readiness
SEPTEMBER 18-19, 2018 | BRUSSELS, BELGIUM | HILTON BRUSSELS GRAND PLACE

DEVICE AND DIAGNOSTIC LABELING WORKSHOP INTENSIVE

Ensuring Swift Collection & Integration of New Labeling Requirements Including the EU MDR & IVDR, Label Management Technology Selection & Optimization
SEPTEMBER 20, 2018 | SAN DIEGO, CA | HILTON GARDEN INN SAN DIEGO DOWNTOWN/BAYSIDE

5TH ANNUAL MEDICAL DEVICE STERILIZATION CONFERENCE

Ensuring the Sterility & Safety of Medical Devices through Robust Validation Practices and Streamlined Compliance Initiatives all while Addressing Increasing Regulatory Scrutiny Surrounding Sterilization Methodology & Ethylene Oxide Residuals
SEPTEMBER 24-25, 2018 | MINNEAPOLIS, MN | MILLENNIUM MINNEAPOLIS HOTEL

LIFE SCIENCE REGULATORY INTELLIGENCE & STRATEGY CONFERENCE

Reducing Risk & Increasing Clearance Certainty through Insightful Regulatory Intelligence & Strategy for Supporting Innovative Study Design Teams to Secure Rapid Product Approval, Expand Indications and Maintain Compliance for Marketed Products
OCTOBER 18-19, 2018 | ALEXANDRIA, VA | SHERATON SUITES OLD TOWN ALEXANDRIA

MEDICAL DEVICE HUMAN FACTORS AND USABILITY CONFERENCE

Developing User-Centered Medical Devices which Maintain Compliance with Regulatory Requirements through Proactive Discovery and Testing of End-User Needs, Deployment of Comprehensive Product Risk Assessment Operations & Execution of Robust Design & Human Factors Validation
OCTOBER 23-24, 2018 | ALEXANDRIA, VA | SHERATON SUITES OLD TOWN ALEXANDRIA

4TH ANNUAL GLOBAL REGULATORY AFFAIRS CMC CONFERENCE

Ensuring Compliant Developmental and Postmarket CMC Operations through the Employment of Thorough Product Lifecycle Management Tactics, Attaining a Comprehensive Understanding of US and Global Regulatory Requirements through to Utilizing Streamlined Processes for Expedited Pathway Approvals
OCTOBER 29-30, 2018 | PHILADELPHIA, PA | DOUBLETREE BY HILTON HOTEL PHILADELPHIA AIRPORT

6TH ANNUAL MEDICAL DEVICE PRODUCT MANAGEMENT CONFERENCE

Evolving Product Management Strategies throughout the Medical Device Lifecycle to Overcome Challenges in Exhibiting Product Value to Healthcare Professionals & Payers, Meet Target Forecasts, Increase Revenue and Organizational Competitiveness
NOVEMBER 7-8, 2018 | CHICAGO, IL

3RD ANNUAL DIETARY SUPPLEMENT: REGULATORY STRATEGY

Alignment with evolving regulations including USDA National Bioengineered Food Disclosure Law, California’s Proposition 65, FDA quality standards & ongoing substantiation of claims highlighting the utilization of social media & influencers.
DECEMBER 3-4, 2018 | ARLINGTON, VA

11TH ANNUAL IVD REGULATORY AFFAIRS CONFERENCE

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 | ARLINGTON, VA

Forums

SEMI-ANNUAL ACO LEADERSHIP FORUM

Driving Excellence & Value in Health Systems | Translating Strategic Vision into Tactical Operations | Aligning Financial Leadership with Corporate Goals
JUNE 12-13, 2018 | JACKSONVILLE, FL | LEXINGTON HOTEL AND CONFERENCE CENTER

SEMI-ANNUAL HEALTHCARE REVENUE CYCLE MANAGEMENT FORUM: CHICAGO

Streamline Front-End Processes to Ensure Rapid & Accurate Reimbursement in an Evolving Landscape Transitioning from Fee-for-Service to Value-Based Care through Leveraging Internal Resources, Technology and Patient Relations
MARCH 7-8, 2019 | CHICAGO, IL

Executive Leadership Support Forums

No Results Found

The page you requested could not be found. Try refining your search, or use the navigation above to locate the post.

Webinars

Share This