Medical Device Industry

With the rapid development 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

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

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 | Alexandria, VA | Hilton Alexandria Old Town

European 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 | Le Meridien Frankfurt Hotel

6th Semi-Annual Medical Device Sterilization Conference: East

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

October 29-30, 2019 | Alexandria, VA | Sheraton Suites Old Town Alexandria

7th Annual Medical Device Product Management Conference

Exploring the Evolution of the Product Manager Role Brought about by the Increase of Global Regulatory Expectations, Strategic Need for Comprehensive Road Mapping Tools and Heightened Importance of Product Launch Initiatives

November 5-6, 2019 | Chicago, IL

10th Semi-Annual EU Medical Device Regulatory Affairs Conference

Focus on the NB Designation 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 | Park Inn by Radisson Brussels Airport

4th Annual EU Medical Device & Diagnostic Quality Management Conference

Ensuring QMS Preparedness in Light of the MDR & IVDR with a Focus on Economic Operator Compliance, Enhanced Supplier Control & Optimal Design of a Robust PMS Strategy, Successfully Managing International Audit Readiness, all while Digitalizing QMS Processes & Data

December 4-5, 2019 | Frankfurt, Germany

EU MDR: Quality System Alignment Conference: Chicago

Implementing Effective and Compliant Quality Management Procedures under the EU MDR through Analysis of Post Market Regulatory Requirements, Risk Mitigation throughout the Supply Chain and Increased Economic Operator Oversight

December 4-5, 2019 | Chicago, IL

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 | Andaz San Diego Hotel

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 | Andaz San Diego Hotel

Regulatory Information Management Systems Conference

Aligning Regulatory Data and Information through Enhanced Integration & Utilization of Regulatory Information Management Systems which Support the Highest Levels of Data Integrity and Seamlessly Support Global Regulatory Documentation from throughout the Product Lifecycle

January 14-15, 2020 | Arlington, VA

6th Annual Medical Device Post-Market Surveillance Conference

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 22-23, 2020 | Alexandria, VA

Medical Device Post Market Clinical Follow-up Conference

Aligning Post Market Clinical Research to Support Regulatory Demands, Generate Evidence to Meet Market Access & Reimbursement Goals through the Selection and Development of Appropriate,
Risk-Based Research Platforms which Deliver Data On-time and On-Budget

January 22-23, 2020 | Alexandria, VA

12th Annual EU Medical Device Clinical Research Conference

Ensuring a Timely & Efficient Approach to Final Steps in Transitioning to MDR Compliant Clinical Strategies Including a Strong Focus on PMCF Requirements, all while Establishing Defined Study End-Points to Optimize Trial Design, Budgeting & Generation of Relevant Quality & Volume of Data

March, 2020 | Amsterdam, NL

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

Tailoring Training Methods & Strategies to Engage Health Care Professionals through Innovative Strategies, Technology & Adaptive Adult Learning Methodologies while Providing Measurable Evaluation on Trainee Retention of Skills, Proficiency & ROI through Value-Driven Metrics

March 31 – April 1, 2020 | San Diego, CA

10th Annual Medical Device Supplier Quality Conference

Assessing and Designating Levels of Risk for a Variety of Suppliers, while Managing the Impact of Regulatory Requirements such as EU MDR, MDSAP, and ISO 13485:2016, in addition to Employing Collaborative Efforts to Validate Supplier Processes and Perform Qualification Audits

April 28-29, 2020 | Arlington, VA

10th Annual Medical Device and Diagnostic Labeling Conference

Streamlining & Optimizing Labeling Strategy in a Rapidly Evolving International Regulatory Environment with a Focus on Developing EU MDR & IVDR Compliant Labels, all while Enhancing Localization & Translation Processes, with the Goal of Reaching Operational Excellence through the Implementation of Impactful ELS, CMS & MDM Technology

May 6-7, 2020 | Chicago, IL

10th Annual Medical Device Packaging Conference

Exploring Robust Testing Methods of Medical Device Packaging, Reviewing Updates and Impact of ISO 11607 and EU MDR, Developing Confident Sampling Plans that Meet FDA Expectations, while Incorporating End User Feedback for Medical Device Packaging Design

May 6-7, 2020 | Chicago, IL

Latest News from our Medical Device Blog

Building a Quality Management Strategy

Melissa Finocchio, Director at bioMerieux, is a featured speaker presenting at the Q1 Productions 4th Annual EU Medical Device & Diagnostic Quality Management Conference.

Achieving Insight through Focused Research

Dr. Russell Branaghan, Professor at Arizona State University, will bring an academic perspective to Q1’s 3rd Semi-Annual Medical Device Human Factors Conference.

Transitioning to the MDR

The Q1 Productions 9th Semi-Annual EU Medical Device Regulatory Affairs Conference takes place September 18-19 in Brussels, Belgium.

Navigating the Last Stages of MDR Implementation

Q1’s 9th Semi-Annual EU Medical Device Regulatory Affairs Conference will cover multiple topics ranging from NB re-designation, to MDR uncertainties and more.

A Note from the Producer: Kayle Pasterz

The sales enablement role within the medical device industry has proven to be buzzworthy, currently influencing curiosity and competition within med device sales teams.

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!

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