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

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 | Le Meridien Frankfurt Hotel

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 | Crowne Plaza Chicago West Loop

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 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

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 Postmarket Surveillance Conference

Ensuring Long-term Product Quality and Efficacy through Streamlined Postmarket Surveillance Processes including Integration of eQMS for Complaint Intake, Employment of Stringent Postmarket Cybersecurity Strategies and Proactively Preparing for EU MDR Compliance

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

Medical Device Software Engineering Conference

Mastering Verification & Validation Challenges for Software as Medical Device as well as Embedded Software by Enhancing Testing Strategies throughout the Product Life Cycle, all while Deploying Agile Methodologies to Software Engineering & Streamlining Quality & Regulatory Compliance

February 25-26, 2020 | San Diego, CA

13th 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

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

April, 2020 | Amsterdam, NL

10th Annual Medical Device Supplier Quality Conference

Updating Supplier Quality Management Processes to Accommodate Innovative Medical Devices, While Collaborating with Software Vendors and Creating Harmonized Systems to Interface with Suppliers on a Global Scale

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

5th Annual Life Science Ethics and Compliance Training Conference

Reducing Compliance Risks through Effective Training Programs and Developing Specific Content Relevant to Each Internal Function and the Overall Organization, while Utilizing Available Resources to Design Innovative Courses in a Cost-Effective Manner

June, 2020 | Chicago, IL

16th Annual Medical Device Coverage and Reimbursement Conference

Aligning Reimbursement Strategies with CMS & Commercial Payer Requirements to Uphold Medical Necessities, Transition from Volume to Value Based Care, Leverage Existing Codes while Overcoming New Code Expectations and Encourage Growth in the Medical Device Industry

July, 2020 | Chicago, IL

5th Annual Medical Device Cybersecurity Risk Mitigation Conference

Ensuring Compliance with Regulatory Requirements and Industry Standards to Mitigate Cyber Risks and Continuously Improve Medical Device Security in addition to Collaborating and Sharing Responsibility between Health Delivery Organizations and Manufacturers

July, 2020 | Arlington, VA

Latest News from our Medical Device Blog

Transitioning to e-beam or X-ray

The 6th Semi-Annual Medical Device Sterilization Conference takes place October 29-30 in Alexandria, VA.

Applying AI and Machine Learning in MedTech

The Q1 Productions 7th Annual Medical Device Product Management Conference takes place November 5-6 in Chicago, IL.

NB Perspectives to Ongoing Regulatory Change

Caroline Dore Geraghty of National Standards Authority of Ireland is a distinguished presenter participating at the Q1 Productions EU Medical Device Post Market Clinical Evaluation Planning Conference this October 29-30 in Frankfurt, Germany.

User-Centered Design for Patients in Home Environments

The 3rd Semi-Annual Medical Device Human Factors & Usability Conference takes place October 22-23 in Alexandria, VA.

Building a Quality Management Strategy

Melissa Finocchio, Director at BioMérieux, 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.

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