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

3RD SEMI-ANNUAL MEDICAL DEVICE STERILIZATION CONFERENCE

Ensuring the Safety & Effectiveness of Medical Devices through the Utilization of Emerging Sterilization Technologies & Validation of Established and Novel Modalities while Addressing Increased Regulatory Scrutiny of Sterilization Practices & Residual Testing
JULY 24-25, 2017 | ARLINGTON, VA

13TH ANNUAL MEDICAL DEVICE COVERAGE AND REIMBURSEMENT CONFERENCE

Securing Coverage via Proactive Collaboration with Private & Commercial Payers to Fulfill Evidence Expectations all while Clarifying HTA Processes, Robust & Impactful Clinical Evidence Generation Strategy Development & Achieving Successful Transitions from Level 3 to Level 1 CPT Codes
JULY 24-25, 2017 | CHICAGO, IL

STRATEGIC LIFE SCIENCE ACCOUNTING & REPORTING CONFERENCE

Innovative Strategies for Transforming Revenue Recognition, Reporting, Financial Planning & Analysis to Drive Revenue, Increase Profitability & Drive Shareholder Value in the New Healthcare Landscape
SEPTEMBER 11–12, 2017 | PHILADELPHIA, PA

MEDICAL DEVICE HUMAN FACTORS AND USABILITY CONFERENCE

Join us in Informing Human Factors & User Needs for Medical Devices while Meeting Regulatory Expectations by Creating Appropriate Risk Assessment Testing, Generating Design Criteria for Efficient Formative & Summative Studies & Accounting for User Needs During R&D
SEPTEMBER 18–19, 2017 | ARLINGTON, VA

LIFE SCIENCE INFORMATION SECURITY CONFERENCE

Ensuring Compliant Handling and Protection of Data, both Patient & Corporate, through Risk-Based Approaches to 3rd Party Assessments, Strong Internal Controls & Proactive Prevention of Breaches through Vulnerability Testing & Incident Response Management
SEPTEMBER 21-22, 2017 | PHILADELPHIA, PA

7TH ANNUAL EU DEVICE AND DIAGNOSTIC REGULATION CONFERENCE

Practical Approaches to the Timely Implementation of MDR-IVDR Regulatory Requirements through the Development & Initiation of a Coherent Transition Framework, Meeting Enhanced Notified Body & Competent Authority Expectations while Eliminating the Risk of Supply Chain Disruption
SEPTEMBER 25-26, 2017 | BRUSSELS, BELGIUM

4TH SEMI-ANNUAL MEDICAL DEVICE STERILIZATION CONFERENCE

Ensuring the Safety & Effectiveness of Medical Devices through the Utilization of Emerging Sterilization Technologies & Validation of Established and Novel Modalities while Addressing Increased Regulatory Scrutiny of Sterilization Practices & Residual Testing
OCTOBER 2-3, 2017 | MINNEAPOLIS, MN

Medical Device Webinars

Latest News from our Medical Device Blog

New Medical Devices Regulation and IVD Regulation Now Published

After more than five years of debate, negotiation and consultation, the new European Medical Device Regulation was published in the Official Journal of the European Union on May 5, 2017, including formal implementation and compliance mandates.

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Sterilization 101

Industry leaders from organizations such as the FDA, CR Bard, and Medtronic will lead solution-driven, in-depth discussions about common industry challenges.

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WannaCry Targets US Medical Devices

The stolen NSA hacking tool that was spread across the world over the weekend, has now infected Medical Devices in the US. It is unclear what hospitals have been affected, but it is confirmed that Bayer Medrad received two reports of their devices being hit by the ransomware.

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A Recap of the Medical Device Packaging & Labeling Summit

Last week, medical device manufacturers from across the U.S. came together to discuss the constantly changing world of labeling at Q1 Productions’ 6th Semi-Annual Medical Device Packaging and Labeling Summit.

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Medical Device and Diagnostic Train the Trainer Summit: Event Recap

Medical Device Train the Trainer Summit Event Recap Engaging Learners | Leveraging Tactile Experiential Education | Effective Course Evaluation By Kate Jeter, Director at Q1 Productions Attending the Annual Q1 Medical Device Train the Trainer Summit is always a...
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When Focusing on Behavior Isn’t Enough

Ergonomics is the study of how humans behave in relation to medical devices. Through the gathering of research and scientific evidence, usability testing is conducted based on the behavior of the end-user.

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How a Label Error Can Ruin a Great Package Design

While the branding of a label on a package is of high importance for any industry manufacturer, overdoing it with branding design and not taking care of the crucial info can cause small to huge errors which can ruin a great package design.

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Eliminating Misconceptions of Cybersecurity

Medical devices, like other computer systems, can be vulnerable to security breaches- potentially impacting the safety and effectiveness of the device. As medical devices are increasingly connected to the Internet, hospital networks, and to other medical devices, this vulnerability becomes more prevalent.

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Harmonizing Medical Device Package Labeling Across Markets

Most Common Symbols and What They Mean

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Understanding ISO 13485: 2016

Understanding ISO 13485: 2016 History, Importance and Implementation Commentary by Kim Trautman There are many compounding factors in the timeline that affect a medical device manufacturer’s decision as to when and how to transition to the new standard ISO 13485:2016....
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CONTACT US
Q1 Productions
500 N. Dearborn Suite 500 | Chicago, IL 60654
Chicago, IL 60654
T: 312.822.8100
F: 312.873.3969
[email protected]

 

 

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