Medical Device Industry

With the rapid developement of new medical devices, the need for continued education is greater than ever. From research and development to marketing and sales, we are here to support you in every step of the product lifecycle.  

Medical Device Conferences

4th Annual Life Science Ethics and Compliance Training Conference

Delivering Training that Reduces Emerging Compliance Risks including Patient Assistance Programs and Off-Label Promotion, Development of Metrics to Gauge Training Effectiveness & Retention, and Considerations in Prioritization of Resources which Ensures Delivery of Highest Level Training in the Most Cost-Effective Manner
June 5-6, 2019 | Chicago, IL | Doubletree by Hilton Chicago O’Hare Airport Rosemont

15th Annual Medical Device Coverage and Reimbursement Conference

Securing Product Reimbursement from CMS & Commercial Payers through Demonstrating Medical Necessity & High Impact Outcomes, Use of Risk Arrangements in Transitioning from Volume to Value-Based Care, Leveraging Existing Codes and Growth in the Medical Device Industry
July 16-17, 2019 | Chicago, IL | Hilton Chicago Magnificent Mile Suites

3rd Annual EU MDR Implementation Conference: Alexandria

Maximizing Remaining Transition Period and Obtaining Product Certification, Development of Adequate Clinical Evaluation Data and Documentation and Clarifying MDR Grey Areas in the Absence of Implementing Acts
July 16-17, 2019 | Alexandria, VA

Life Science Advertising and Promotion Regulatory Affairs Conference

Reducing Risks & Increasing Effectiveness of Advertising & Promotion through Advertising & Promotion Regulatory Oversight, Interpreting & Implementing FDA Guidance on Medical Product Communications That Are Consistent With the FDA-Required Labeling and Guidance on Drug & Device Manufacturer Communications With Payors, Formulary Committees & Similar Entities
July 23-24, 2019 | Arlington, VA

4th Annual Medical Device Cybersecurity Risk Mitigation Conference

Mitigating Cybersecurity Risks through Implementing Regulatory Standards and Industry Frameworks while Increasing Collaboration between Manufacturers and Health Delivery Organizations to ensure Proactive Approaches to Device Security
July 23-24, 2019 | Arlington, VA | Le Meridien Arlington

Medical Device and Diagnostic Sales Enablement Conference

Increasing Overall Efficiency and Effectiveness of Medical Device Sales Teams through Exploration of Internal Commercial Alignment and Communication, Employment of Innovative Technologies for Streamlined Content Delivery and Training, and Promotion Cross Functional Collaboration for Optimal Sales Operations and Future Sales Enablement
July 23-24, 2019 | Chicago, IL

8th Annual Life Science Strengthening Patient Advocacy Engagement Conference

Enhancing Patient Advocacy Initiatives through an Increased Focus on Diverse Patient Populations and Comprehensive Alliance Building Efforts While Strategizing for Innovative and Improved Access Opportunities, Optimizing Data Circulation and Partnering for Patient Success
July 30-31, 2019 | Philadelphia, PA | Four Points by Sheraton Philadelphia City Center

9th Annual Medical Device Pricing and Strategic Accounts Conference

Establishing & Building Strategic Partnerships with Key Customers, Focusing on Value and Contract Effectiveness with the use of Advanced Pricing Models, Knowledge of Impactful Healthcare Economics, While Overcoming Competition and Transparency with the use of Benchmarking Data
September 10-11, 2019 | Charlotte, NC

9th European Medical Device Regulatory Affairs Conference

Focus on the NB Redesignation Status & Timeline, Rationale for Prioritization of Specific Product Line Compliance with New Rules & Management of Remaining Tasks, all while Addressing Ongoing MDR Uncertainties in Finalizing the Updated Regulatory Strategy
September 18-19, 2019 | Brussels, Belgium

Life Science Manufacturing Automation Optimization Conference

Ensuring Robust, Uninterrupted, and Compliant Product Supply Chains through Facility Retrofitting to Integrate Industry 4.0 Capabilities and Connected Software Systems, Embracing IoT, and the Utilization of Cutting Edge Instrumentation
September 24-25, 2019 | Charlotte, NC

3rd Semi-Annual Medical Device Human Factors & Usability Engineering Conference

Aligning Human Factors & Usability Studies with Expanding Requirements including the Lifecycle of FDA Regulatory Documentation, CE Mark Changes in Light of EU MDR and ISO 62366, Designing and Conducting Comprehensive and Coherent Studies that Provide Accurate Use Data all while Propelling User Needs into the Forefront of Design & Development
October 22-23, 2019 | Arlington, VA

EU Medical Device Post-Market Clinical Evaluation Planning Conference

Developing & Implementing Robust Plans to Gather Compliant Post-Market Clinical Follow-Up Data, Practically Defining Clinical Evidence Based on Device Class & Acceptable Information, all while Sharing Solutions to Operational Challenges in Cost-Effective Data Collection
October 29-30, 2019 | Frankfurt, Germany

6th Semi-Annual Medical Device Sterilization Conference

Industry Collaboration & Consensus on Ethylene Oxide Residual Reduction, Risk-Based Approaches to Selection & Validation of Sterilization Modality to Meet Increasingly Complex Regulatory Requirements including FDA Parametric Release, Numerous ISO Standards and EU MDR
October 29-30, 2019 | Arlington, VA

7th 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 2019 | Chicago, IL

4th Annual European Medical Device Quality Assurance Conference

Best Practices in Handling Regular & Unannounced Audits, Addressing MDR & IVDR Developments & Impact on Quality Assurance Operations, all while Exploring Efficient Strategies in Change Control Management & Process Validation
November 2019 | Berlin, Germany

4th Semi-Annual Medical Device Human Factors & Usability Engineering Conference: West

Aligning Human Factors & Usability Studies with Expanding Requirements including the Lifecycle of FDA Regulatory Documentation, CE Mark Changes in Light of EU MDR and ISO 62366, Designing and Conducting Comprehensive and Coherent Studies that Provide Accurate Use Data all while Propelling User Needs into the Forefront of Design & Development
December 10-11, 2019 | San Diego, CA

7th Semi-Annual Medical Device Sterilization Conference: West

Industry Collaboration & Consensus on Ethylene Oxide Residual Reduction, Risk-Based Approaches to Selection & Validation of Sterilization Modality to Meet Increasingly Complex Regulatory Requirements including FDA Parametric Release, Numerous ISO Standards and EU MDR
December 10-11, 2019 | San Diego, CA

13th Semi-Annual Medical Device Clinical Training & Education Conference

Designing & Executing Innovative, Engaging HCP Training which Incorporates Adaptive Adult Learning Methodologies & Technology to Increase Retention while Providing Measurable Return on Investment which Evaluates Competency, Skills & Proficiency through Value-Driven Metrics
March 31 – April 1, 2020 | San Diego, CA

14th Semi-Annual Medical Device Clinical Training and Education Conference

Designing & Executing Innovative, Engaging HCP Training which Incorporates Adaptive Adult Learning Methodologies & Technology to Increase Retention while Providing Measurable Return on Investment which Evaluates Competency, Skills & Proficiency through Value-Driven Metrics
May 12-13, 2020 | Charlotte, NC

Latest News from our Medical Device Blog

2019 Medical Device and Diagnostic Industry Trends

View the full 2019 Industry Trends report to hear from industry peers on how organizations are adapting to prepare for continued growth and development.

Panel Preview: Reaching Success In Partnerships With Translation Providers

Anita Stever, Senior Technical Writer at ACIST Medical Systems and Sara Brouillette, Senior Global Labeling Specialist at bioMérieux share insights on their upcoming panel.

Understanding GUDID

Dawn Fowler, Director, UDI/Master Data Management at Masimo shares insight into her presentation at the 9th Annual Medical Device & Diagnostic Labeling Conference.

The Fundamentals of Salesmanship

ulie Young and Carol Keohane of Olympus and Steve Emerson are participating in Q1’s 12th Annual Medical Device & Diagnostic Sales Training & Development Conference on February 26-27 in Charlotte, NC.

Session Preview: Deep Dive Into The Medical Device Single Audit Program (MDSAP)

Paul Chiappetta is the Director, Quality Systems and Compliance at Thermo Fisher Scientific. He is presenting at the upcoming Medical Device Supplier Quality Conference on April 29-30 in Arlington, VA. Learn more about his presentation below!

Session Preview: Effective Field Sales Training Programs

Susan Rapoza is a Director of Sales Training and Chris Cassell, CPTM, is a Sales Training Manager at Align Technology. Their presentation, “Increasing the Effectiveness of Field Sales Training Programs,” will be featured at Q1 Productions’ upcoming 12th Annual Medical Device & Diagnostic Sales Training & Development Conference.

What’s in an Age?

Marilyn Burns is the Director of Clinical Affairs at Symmetry Surgical. She is presenting at the upcoming Medical Device Clinical Training Conference on February 26-27 in Charlotte, NC. Learn more about her presentation below!

Managing The Time Crunch: Best Practices, Solutions & Ideas

Greg Prevatt is the Director of Education at Apollo Endosurgery and is presenting at the upcoming Medical Device Clinical Training Conference on February 26-27 in Charlotte, NC. Learn more about his presentation below! Can you give a brief overview of your role at...

So You Want to Break Into the Medical Device Industry…

Amazon recently made news for its long-anticipated announcement of Amazon HQ2, its two new locations in New York City and Crystal City, VA. While the 14-month search process and bidding process was raising concern and buzz, there was another Amazon story that was...

Beep…Boop…Bop: Redesigning the Sounds of Medical Devices

Human Factors and Usability professionals have the unique understanding of how healthcare professionals can and do use medical products in a real-world setting. The art and science of developing medical devices that patients can properly interact with and...

CONTACT US
Q1 Productions
500 N. Dearborn Suite 500 | Chicago, IL 60654
Chicago, IL 60654
T: 312.822.8100
F: 312.873.3969
marketing@q1productions.com

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