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

6TH SEMI-ANNUAL MEDICAL DEVICE SUPPLIER QUALITY CONFERENCE WEST

The #1 Gathering for Medical Device Supplier Quality Teams to Exchange Progressive Ideas for Implementing a Risk-Based Approach to Supplier Monitoring in Compliance with ISO 13485 while Actualizing Efficiencies in Supplier Audits, Sub-Tier Supplier Management & Supplier Development
JUNE 5-6, 2017 | SAN JOSE, CA

EUROPEAN MEDICAL DEVICE REGULATION CONFERENCE

Clarifying Critical Provisions from the EU MDR & Addressing Evolving Collaborations with Notified Bodies, all while Conducting Regulatory Gap Assessments & Initiating In-House Strategy Revisions
JULY 13-14, 2017 | ALEXANDRIA, VA

2ND ANNUAL MEDICAL DEVICE CYBERSECURITY RISK MITIGATION CONFERENCE

Analysis & Clarification of the FDA Post-Market Device Cybersecurity Management Guidance, Continuously Identifying Vulnerabilities & Ensuring Robust Threat Response Strategies all while Proactively Integrating Cybersecurity into Device Design
JULY 17-18, 2017 | ARLINGTON, VA

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 | ALEXANDRIA, 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

MEDICAL DEVICE HUMAN FACTORS AND USABILITY CONFERENCE

Join us in advancing the role of patient advocacy through improved collaboration with advocacy organizations, strategically measuring and benchmarking advocacy initiatives to increase support while empowering the patient community. This exciting annual meeting seamlessly blends robust educational content alongside informal networking.
SEPTEMBER 18–19, 2017 | ARLINGTON, VA

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

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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Brexit

On June 23, 2016, the UK voted to withdraw from the European Union, raising many questions about the future of clinical trials. However, Brexit wasn’t the beginning of the conversation, and it certainly isn’t the end.

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5 Things to Consider When Choosing a Supplier

Top Five Things to Consider When Choosing your Supplier We Asked Industry Experts. Here’s What We Found. As medical devices become increasingly complex, the need for reliable, compliant, and cost-efficient supplier partners is of great importance to strategic...
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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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