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

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 22-23, 2020 | Amsterdam, NL

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

2nd Annual Life Science Digital Transformation Conference

Optimizing Digital Transformation Initiatives to Reach Defined Objectives, Effectively Engaging with Stakeholders to Lead an Organization-Wide Cultural Shift, all while Focusing Digitalization Efforts on Greater Consumer Data Collection & Processing Capabilities

May 19-20, 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

7th Annual Customer Centric Medical Information Conference

Optimizing Medical Information Operations and Inquiry Responses through the Integration of AI and Automation Tools, Evolving the Standard Response Letter and Utilizing Data Analytics to Ensure Impactful Product Message Development

July, 2020 | Boston, MA

11th 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, 2020 | Brussels, Belgium

5th Semi-Annual Medical Device Human Factors & Usability 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, 2020 | Arlington, VA

8th Semi-Annual Medical Device Sterilization Conference: East

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, 2020 | Arlington, VA

8th Annual Medical Device Product Management Conference

Instilling Comprehensive Road Mapping Tools for Heightened Portfolio Success to Lead Strategic Launch Initiatives and Evolve in an Ever-Changing Landscape while Forecasting Trends with AI Based Products

October 27-28, 2020 | Chicago, IL

2nd Annual 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

November, 2020 | Chicago, IL

12th 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

November, 2020 | Brussels, Belgium

5th Annual EU Medical Device and 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, 2020 | Frankfurt, Germany

9th 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, 2020 | San Diego, CA

6th 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, 2020 | San Diego, CA

Latest News from our Medical Device Blog

An Interview With Donna Carlson

Donna Carlson, Principal Software Quality Engineer at Medtronic (Louisville, Colorado), is a featured speaker presenting at the inaugural Medical Device Software Engineering Conference. The event takes place on February 25-26 in San Diego, CA, where several industry...

Best Practices for Adverse Event Monitoring

Jacqui Budde will be presenting at the upcoming Medical Device Postmarket Surveillance & Clinical Follow-Up Conference in Alexandria on January 22-23.

Meeting MDR Expectations for Post Market Activities

Eric Henning from DEKRA Certification B.V. is one of several speakers presenting at the upcoming Medical Device Postmarket Surveillance & Clinical Follow-Up Conference taking place January 22-23 in Alexandria, VA.

Conveying Value of Clinical Training Programs

Phillip Modesti, Senior Director of Medical Education at Hologic is a featured speaker presenting at the West Coast Medical Device Clinical Training & Education Conference.

Session Preview: EU MDR Quality System Alignment Conference

Jon Cornell, Head of Quality at Coloplast is a featured speaker presenting at the inaugural EU MDR: Quality System Alignment Conference.

Portfolio Management of Legacy Products

Thursday, January 23, 2020 | 12:00 PM – 12:40 PM CST

Validation Failure: Cause, Avoidance and Recovery

Natalie Abts, Head of Human Factors Engineering at Genentech is one of the many leading speakers at the upcoming Medical Device Human Factors and Usability Conference.

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.

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