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Webinars

Materials for Implantable Devices

Selecting the right materials when designing an implantable medical device is critical to funcationality, long-term performance, and patient safety. In this webinar, you will learn about the unique challenges medical device designers must overcome, and how how to select the right TPU grade for your specific in-the-body application.

Wed, June 19, 2019 – June 19, 2020(all day)

Duration: 15 minutes

Sponsored by Lubrizol LifeSciences


Integrator's Guide to SpO2 Solutions

Before adding new parameters to integrated monitoring systems, original equipment manufacturers have several  decisions to make. This presentation will help product development engineers and project managers understand the requirements and challenges of integrating pulse oximetry technology.

Thurs, May 30, 2019 - May 30, 2020(all day)

Duration: 20 minutes

Sponsored by Nonin


How to Prepare for EU MDR 2020 

In less than one year, the Medical Devices Regulation (MDR) will be fully implemented. As of May 2020, medical device manufacturers that wish to distribute products in the European Union will be required to comply with these new rules.  For these organizations, there is a lot to do to prepare in a relatively short time.  In this webinar, you’ll learn valuable insight from industry experts and medical device manufacturers on how to be fully prepared for this important regulatory change.  

Wednesday, May 29, 2019(all day)

Duration: 60 minutes

Sponsored by etq


Overcoming Design Challenges with Novel Resorbable Biomaterials

This webinar from Secant Group, LLC, a leading producer of resorbable poly(glycerol sebacate) (PGS) resin, offers guidance for overcoming key design challenges with resorbable biomaterials on the journey to commercialization. These challenges include navigating the biomaterials market, identifying the ideal properties of a biomaterial, addressing compliance mismatch, protecting intellectual property, and knowing when to start working with the FDA. 

Wednesday, May 1, 2019 - May 1,  2020(all day)

Duration: 36 minutes

Sponsored by Secant Group


Microsized Extrusion Concepts

Learn how low durometer, thin walled extrusion can contribute to cost efficiencies and safer devices that could help your medical device company keep up with minimally invasive devices.

Wednesday, May 8, 2019

Duration: 50 minutes

Sponsored by Flexan


Looking for a safer, smaller, energy dense battery for your medical device?

Design Engineers are continuing to innovate in the medical device markets; developing smaller, yet more powerful devices. A primary challenge the designers face is how to miniaturize a device around the large batteries previously required for such applications. ZPower has developed the answer. The ZPower silver-zinc rechargeable cell is the smallest, high-energy density microbattery available; enabling a new generation of products, including many new hearable medical device products, by providing over 58 mWh in packages smaller than the collar button of a dress shirt. ZPower batteries are also non-flammable and non-toxic making them the safest way to power next generation medical device products. This webinar is intended to provide design engineers with greater detail on the benefits of integrating ZPower’s rechargeable microbatteries into their own designs and how ZPower can support that effort.

Tues, April 30, 2019

Duration: 60 minutes

Sponsored by: ZPower


Biocompatibility: Applying the New ISO 10993 Standards

A new updated ISO 10993-1 standard came out in Aug of 2018 that drastically changed how we access medical devices for biocompatibility. We're also dealing with the impact of the Medical Device Regulations in Europe. The timing of these two documents has greatly disrupted the medical device industry. In this webinar we will discuss the changes and efficient approaches to navigate through the troubles. 

Thurs, April 11, 2019

Duration: 46 minutes

Sponsored by Nelson Labs


A Complaint Management Primer: Compliance-Driven Strategies for Effective Complaint Management

Medical device complaint handling and adverse event reporting has been required since the first iterations of ISO 13485 and FDA guidance for quality systems. Yet, complaint management practices continue to be the top reasons for FDA 483 observations and warning letters.  This webinar will discuss strategies for implementing a complaint management process that facilitates gathering, evaluating, investigating and remediating complaints from the premarket stage to closure–and what practices to avoid. 

Tues, March 19, 2019

Duration: 30 minutes

Sponsored by: AssurX


Med Tech Trends: Innovation and Adaptation

The medtech industry continues to grow though at a much slower pace than the previous decade. The industry’s long-term outlook is at risk due to underinvestment in digital capabilities, competition from technology and retail companies, and the growing need to demonstrate better outcomes. This webinar will keep you informed of recent trends in the medtech industry to stay competitive. 

Thurs, November 29, 2018