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

4TH ANNUAL MEDICAL DEVICE STRATEGIC SOURCING CONFERENCE

Ensuring Cost Effectiveness through the Strategic Implementation of Cost Modeling, Negotiation and Regulatory Compliance while Implementing Innovative Technology and Sourcing for Continuity
APRIL 23-24, 2018 | HERNDON, VA | HILTON WASHINGTON DULLES AIRPORT HOTEL

7TH SEMI-ANNUAL RISK BASED MEDICAL DEVICE SUPPLIER QUALITY ASSURANCE CONFERENCE

Holistic, Risk-Based Approaches to Supplier Qualification, Monitoring & Performance Evaluation to Meet Regulatory Standards including ISO 13485:2016 and the Medical Device Single Audit Program, Ensuring Global Compliance & Highest Quality Products
APRIL 23-24, 2018 | HERNDON, VA | HILTON WASHINGTON DULLES AIRPORT HOTEL

8TH ANNUAL MEDICAL DEVICE AND DIAGNOSTIC LABELING CONFERENCE

Label Management Technology Selection & Optimization to Reach Label Creation & Delivery Excellence, Ensuring Swift Collection & Integration of New Labeling Requirements Including the EU MDR & IVDR, Achieving UDI Barcode Quality & Direct Marking
MAY 15-16, 2018 | CHICAGO, IL | HILTON CHICAGO – MAGNIFICENT MILE SUITES

8TH ANNUAL MEDICAL DEVICE PACKAGING CONFERENCE

Elevating Package Design of Medical Devices by Incorporating End User Feedback, Robust Testing Methods and Use of Innovative Materials to Reduce Cost, Ensure Safety and Surpass Regulatory Expectations
MAY 15-16, 2018 | CHICAGO, IL | HILTON CHICAGO – MAGNIFICENT MILE SUITES

3RD ANNUAL LIFE SCIENCE COMPLIANCE TRAINING CONFERENCE

Mitigating the risk of compliance enforcement action through the development and delivery of highly effective compliance training that engages employees on a global level, ensuring alignment with corporate standards and regulatory requirements.
JUNE 6-7, 2018 | CHICAGO, IL

14TH ANNUAL MEDICAL DEVICE COVERAGE AND REIMBURSEMENT CONFERENCE

Blending stakeholder perspectives including payer medical directors & contracting executives with hospital purchasing and IDN value analysis committees alongside innovative medical device manufacturers securing coverage and reimbursement for medical technologies throughout the spectrum of care in an uncertain and evolving environment.
JULY 11-12, 2018 | CHICAGO, IL

2ND ANNUAL EU MDR IMPLEMENTATION CONFERENCE

Securing Corporate Buy-In & Deploying the Regulatory Transition Plan as a Business Project In-depth Analysis of the NB Redesignation Process & the Impact on Recertification Timelines Practical Approach to Implementing New EU Clinical & Post-Market Requirements
JULY 12-13, 2018 | ALEXANDRIA, VA

3RD ANNUAL MEDICAL DEVICE CYBERSECURITY RISK MITIGATION CONFERENCE

Proactive Integration of Cybersecurity Measures throughout the Medical Device Lifecycle Deploying a Robust Cybersecurity Compliance Strategy to Meet FDA Expectations Engaging with HDOs to Optimize Cybersecurity in the Hospital Environment
JULY 16-17, 2018 | ARLINGTON, VA

7TH ANNUAL PATIENT ADVOCACY ENGAGEMENT CONFERENCE

Elevating Patient Advocacy through Creative, Patient-Centric Approaches to Engage with Advocacy Groups and Patients Directly, Ensuring Integration of the Patient Voice, Deep Levels of Comprehensive Support and Highest Levels of Value and Return on Investment
JULY 17-18, 2018 | BALTIMORE, MD

5TH ANNUAL CUSTOMER CENTRIC MEDICAL INFORMATION CONFERENCE

Enhancing Medical Information Operations through Comprehensive Data Mining and Analytical Analysis Strategies to Improve Information Outreach, Harmonization of Messaging across Global Landscape and Patient Advocacy Perspective to Increase Impact of Medical Information Content
JULY 23-24, 2018 | BOSTON, MA

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

Medical Device Webinars

Latest News from our Medical Device Blog

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).

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.

Top Challenges in Strategic Sourcing and How to Combat Them

The ultimate goal of those involved in sourcing and procurement is to procure components for the best value possible.

Is IoT Technology Making the Internet Irrelevant?

As information technology continues to develop and reinvent itself, old technology is declared irrelevant and replaced. The same can be argued for the Internet.

How Clinical Education Will Evolve in the Next 5 Years

How Clinical Education Will Evolve in the Next 5 Years Clinical Training and Education is an industry that faces many unique challenges. Educating customers on technical, clinical, and procedural uses of medical devices is an essential component of running a...

Preparing For Your Clinical Evaluation Report

Preparing For Your Clinical Evaluation Report Aligning with MEDDEV 2.7.1 and the MDR The newest revision has defined, clarified and tightened guidance on clinical evidence requirements for unapproved technologies as well as products that have been on the market for an...

4 Steps to Deploy a Cybersecurity Postmarket Strategy

While the development of innovative technologies and connected devices continues to flourish, public concern surrounding cybersecurity has increased significantly in recent years.

Tips from Corporate Strategy Experts

As the medical device industry changes, companies are looking to achieve sustainable growth and business development.

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).

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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