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

12TH SEMI-ANNUAL LIFE SCIENCE CFO STRATEGIC GOVERNANCE FORUM

Driving Excellence & Profitability Across the Life Science Industry through Translating Strategy & Executive Vision into Tactical Financial Operations, Transforming Financial Leadership & Development to Ensure Long-Term Success
JUNE 14-15, 2018 | BOSTON, MA | HILTON BACK BAY

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 | COURTYARD CHICAGO DOWNTOWN MAG MILE

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 | ARLINGTON, VA | HYATT CENTRIC ARLINGTON

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 | KEY BRIDGE MARRIOTT

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 | LORD BALTIMORE HOTEL

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

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

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

2ND ANNUAL MEDICAL DEVICE HUMAN FACTORS AND USABILITY CONFERENCE

Developing User-Centered Medical Devices while Maintaining Compliance with Regulatory Requirements through Proactive Discovery of End-User Needs, Employment of Comprehensive Product Risk Assessment Operations, and Execution of Robust Validation Strategies
OCTOBER 23-24, 2018 | ARLINGTON, VA

Medical Device Webinars

Latest News from our Medical Device Blog

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...

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...

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.

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.

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