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

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 | PARK INN BY RADISSON BRUSSELS AIRPORT

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 | CROWNE PLAZA NORTHSTAR HOTEL

5TH ANNUAL MEDICAL DEVICE PRODUCT MANAGEMENT CONFERENCE

Establishing Product Management’s Impact on the Bottom-Line through Aligned Upstream & Downstream Activities and Execution That Incorporates End-User Feedback and the Continuous Evolution of the Healthcare Environment
OCTOBER 23-24, 2017 | CHICAGO, IL

LIFE SCIENCE INSPECTION READINESS CONFERENCE

Proactively Planning & Executing Successful Quality Inspections through Subject Matter Expert Training Excellence, Standard Procedures & Protocols to Ensure Optimal Data Integrity, and Comprehensive Education in Regulatory Authority Audit Expectations
NOVEMBER 6-7, 2017 | ARLINGTON, VA

4TH ANNUAL MEDICAL DEVICE GLOBAL POST-MARKET SURVEILLANCE CONFERENCE

Ensuring User Feedback & Complaints are Handled Appropriately and Aligned with US and International Regulatory Requirements, Streamlining and Improving Decision Making, Response Times, and Ultimately Ensuring the Safety & Quality of Medical Products
JANUARY 18-19, 2018 | ARLINGTON, VA

Medical Device Webinars

Latest News from our Medical Device Blog

Sterilization Recap

The following is a Q&A, featuring attendee feedback from the 3rd Semi-Annual Medical Device Sterilization Conference

EU MDR Whitepaper: Quality Management Systems

The MDR contains explicit requirements for manufacturers to establish, implement, and manage a quality management system (QMS).

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.

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.

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.

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.

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...

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.

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.

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.

CONTACT US
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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