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

11TH ANNUAL MEDICAL DEVICE AND DIAGNOSTIC SALES TRAINING AND DEVELOPMENT CONFERENCE

Executing highly effective training & development in an evolved, value-based sales environment, creating and engages sales force through supportive & impactful training from onboarding to established representatives through leverage of technology, blended learning and skills development, delivering return on investment & a dynamic, seamless sales force
FEBRUARY 22-23, 2018 | PHOENIX, AZ | POINTE HILTON TAPATIO CLIFFS RESORT

11TH ANNUAL MEDICAL DEVICE CLINICAL TRAINING AND EDUCATION CONFERENCE

Delivering Effective Training that Engages a Range of Healthcare Professions through Impactful Blended Training & Education programs that Utilize Experiential Learning and Technology, to accomplish Defined Learning Objectives that Ensure Learner Retention and Return on Investment
FEBRUARY 22-23, 2018 | PHOENIX, AZ | POINTE HILTON TAPATIO CLIFFS RESORT

10TH ANNUAL EU MEDICAL DEVICE CLINICAL RESEARCH CONFERENCE

Aligning Clinical Strategies with MDR & MEDDEV Regulatory Requirements, Obtaining a Greater Volume of Clinical Data to Support Regulatory & Access Goals, Integration of Unique Initiatives such as IIS to Broaden Indications & Maintain Budgets
MARCH 20-21, 2018 | BERLIN, GERMANY | MELIA BERLIN

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

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

3RD ANNUAL MEDICAL DEVICE CYBERSECURITY RISK MITIGATION CONFERENCE

Continuous Identification of Vulnerabilities to Ensure Robust Threat Response Strategies, Interpretation of FDA Post-Market Cybersecurity Guidance with Practical Steps for Updating Equipment & Proactive Integration of Cybersecurity Risk Management into Medical Product Design & Development
JULY 2018 | ARLINGTON, VA

14TH ANNUAL MEDICAL DEVICE COVERAGE AND REIMBURSEMENT CONFERENCE

Blending Stakeholder Perspectives including Payer Medical Directors & Contracting Executives with Hospital Purchasing & IDN Value Analysis Committees alongside Innovative Medical Device Manufacturers, Securing Coverage & Reimbursement for Medical Technologies throughout the Spectrum of Care in an Uncertain & Evolving Environment
JULY 11-12, 2018 | CHICAGO, IL

MEDICAL DEVICE TECH FORUM

Achieving Excellence in Technology Integration | Translating Strategy & Vision into Tactical Implementation | Transforming Leadership & Executive Support
JULY 19, 2018 | MINNEAPOLIS, MN

Medical Device Webinars

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Latest News from our Medical Device Blog

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).

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.

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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