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

8TH ANNUAL MEDICAL DEVICE STRATEGIC PRICING CONFERENCE

Blending Stakeholder Perspectives including IDN, Health System & GPO Contracting Decision Makers with Industry Expert Utilizing Advanced Pricing Models to Leverage Risk Agreements, Overcoming Competition & Transparency Concerns in an Evolving Reimbursement & Health Policy Environment
SEPTEMBER 11-12, 2018 | CHARLOTTE, NC | CHARLOTTE MARRIOTT SOUTHPARK

8TH ANNUAL MEDICAL DEVICE CONTRACTING AND STRATEGIC ACCOUNTS CONFERENCE

Establishing and Building Relationships with Key Customers through Increased Value Metrics and Contract Effectiveness, while Leveraging GPOs and Increasing Risk Share to Maintain an Advantage in a Highly Competitive Market
SEPTEMBER 11-12, 2018 | CHARLOTTE, NC | CHARLOTTE MARRIOTT SOUTHPARK

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

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

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 | ARLINGTON, VA

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

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WEBINAR: Best Practices for Medical Device Reporting (MDR) Under FDA’s Final Guidance

WEBINAR: Status Update- MDR Surprises and Key Regulatory Developments

Medical Device Webinars

Latest News from our Medical Device Blog

Navigating the Evolving Pricing Landscape

Over the past decade, there has been a significant shift in medical device purchasing, pricing, reimbursement and support. Several professionals in this industry, including medical device manufacturers, health systems, as well as patients have had to adjust to the...
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Can UX Save Lives?

Human factors and usability testing professionals play an integral role during medical device design and post-market operations. In order to ensure medical devices are intuitive for HCP and patient use, human factors teams must develop safety validation strategies and...
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Exploring 5 Trends in Enterprise Labeling

Navigating and staying ahead of the curve in the labeling industry can be challenging. There are evolving technologies, regulations and trends to keep in mind. Manufacturing.net recently published a two-part article that explores the challenges within enterprise...
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What’s Next? Brexit, Medical Devices and Beyond

As regulatory professionals continue to adapt to EU’s Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR), another challenge that many in the medical device industry face is the reality of Brexit. As a result of the changing regulations, there is...
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The War on Germs: How Robots are Revolutionizing Sterilization

When we think of hospitals and healthcare facilities, many tend to think about how these places are havens of cleanliness and sterility. And while this is generally a fact, according to a recent CDC report on Healthcare-Associate Infections (HAIs), “On any given day,...
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How The VA Is Improving Cybersecurity

It’s no surprise that organizations across industries are taking measures to ensure top medical device cybersecurity for their clients, customers and products. Government entities are certainly no strangers to this process. The Department of Veterans Affairs recently...
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Impact of EU MDR on Notified Bodies

As medical device companies are beginning to transition towards the EU Medical Device Regulation standards, there is no denying that Notified Bodies are also making strides to meet the May 2020 deadline. According to a recent article, the new regulations include...
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Understanding the FDA Cybersecurity Go-Team

The U.S. Food and Drug Administration (FDA) recently unveiled the Medical Device Safety Action Plan: Protecting Patients, Promoting Public Health, a comprehensive plan with the goal of assessing processes and procedures in order to enhance medical device security in an ever-evolving technological landscape.

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From On-Screen To Real Life

The US Food and Drug Administration (FDA) recently released a new medical device safety action plan that contains five focus areas that aim to improve the quality of real-world evidence, improve post-market surveillance, spur innovation around safer devices, advance cybersecurity initiatives and reorganize the Center for Devices and Radiological Health (CDRH).

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5 Things to Consider When Choosing a Supplier

As medical devices become increasingly complex, the need for reliable, compliant, and cost-efficient supplier partners is of great importance to strategic sourcing and direct procurement executives.

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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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