Webcasts

MD+DI regularly produce webinars and online courses on a wide variety of topics important to medical device professionals. Check back regularly for upcoming webinars and online courses as well as watching the on demand versions listed below.

Upcoming Webinars and Online Courses

Practical Risk Management: How to Integrate ISO 14971 into your Product Development Lifecycle

Medical device risk management using ISO 14971 has become an industry best practice for medical device manufacturers. Adopting ISO 14971 methodology may become burdensome or complex if elements such as risk planning, risk analysis, risk reporting, and postmarket risk surveillance are implemented poorly.

This practical course will highlight key deliverables and how to generate them, reference warning letters and 483s for examples of what and what not to do, and identify when and how to integrate risk management with the typical medical device product development lifecycle.

Learn from David Amor, an industry consultant who specializes in helping companies such as Boston Scientific, St. Jude Medical, and smaller startups navigate through FDA remediation activities surrounding risk management.

Date: April 28 - 30, 2015
Time: 11:00 AM PT / 2:00 PM ET
Duration: 60 minutes

Sponsored by:
Arena Solutions

Hosted by:
Qmed Logo

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Featured Webinars

The Lifecycle of a UDI Record - Submission is only the beginning

This webcast gives device labelers a different perspective on UDI submission. Rather than being an endpoint, UDI submission is the start of a living record – that has a lifecycle. The presentation also examines the long term benefits of UDI data as persistent, living records for use across sectors of the life sciences industry. These UDI records will be a key building block in the drive toward global healthcare interoperability.

Date: May 15, 2015
Time: 8:00 AM PT / 11:00 AM ET
Duration: 10 minutes

Sponsored by:
Reed Techn

Hosted by:

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Make vs. Buy – A Model for Performing this Analysis

When an idea for a new medical device – or reinvention of an obsolete one – arises, it can be difficult to decide its development and manufacturing destinations. Does your company have the necessary resources to take on that kind of challenge, or is it more economical to begin research on Contract Manufacturers? Essentially do you make, or do you buy? How do you choose?

Date: February 17, 2015
Time: 8:00 AM PT / 11:00 AM ET
Duration: 60 minutes

Sponsored by:
Arena Solutions

Hosted by:

Watch Now!


Archived and On-Demand Webcasts

The following webcasts are available on demand. Follow the links to access archived content.

The Secret to Accelerated Innovation AND Increased Compliance

In today’s increasingly complex market, some medical device companies fear stricter regulatory standards will compromise their ability to accelerate innovation. Fortunately, that is not true. Solid design control business practices coupled with a modern product design solution can ensure medical device companies — even those with globally disseminated supply chain teams — achieve compliance without sacrificing accelerated innovation. Join Topera’s Quality Assurance Director Ken Perino and Arena Solution’s Validation Program Manager Yelena Bolton to learn how medical device companies are balancing business and compliance with their design control process.

Date: January 21, 2015
Time: 11:00 AM PT / 2:00 PM ET
Duration: 60 minutes

Sponsored by:
Arena Solutions

Hosted by:

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Biocompatibility: Rethinking the New Big Three (Cytotoxicity, Sensitization & Irritation Testing)

This webinar will examine how the “Big Three” biocompatibility tests (cytotoxicity, sensitization, and irritation) are advancing and what those advancements mean for medical device manufacturers. In addition to the Big Three, course registrants will learn about the in vitro sensitization/irritation testing model, and what is being done to ensure regulators accept in vitro alternatives. Additionally, registrants will receive insight into the value of in vitro testing as a means of reducing testing costs, and accelerating time to market.

Date: November 20, 2014
Time: 11:00 AM PT / 2:00 PM ET
Duration: 60 minutes

Sponsored by:
Neslon Laboratories

Hosted by:

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Choosing the Right System Software for Medical Devices

Join Stephen Olsen, Product Line Manager for VxWorks and Neil McLellan, Senior Product Manager, Medical Platforms, for Wind River as they cover areas that software developers and manufacturers need to consider when choosing the right system software for medical device applications.

Date: October 7, 2014
Time: 11:00 AM PT / 2:00 PM ET
Duration: 60 minutes

Sponsored by:

Wind River

Hosted by:

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How Medical Device Manufacturers Control Their Supply Chain and Achieve Compliance

Medical Device companies are innovating faster than ever. New technologies and materials are behind the wave. It all comes down to staying in control. Strict control over design history, product lifecycle management, comprehensive change control processes, and proactive supply chain risk analysis are key to success. In this webinar, you'll learn — from three very unique perspectives — the keys to achieve compliance, reduce product risks, and maximize business results.

Date: September 17, 2014
Time: 9:00 AM PT / 12:00 PM ET
Duration: 60 minutes

Sponsored by:

Arena Solutions

Hosted by:

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Improving Medical Devices and Advanced Technologies through Conformal Coatings

Heightened demands for improved product reliability are often addressed through the use of high-quality conformal coatings. Poly(para-xylylene), known as Parylene, is an ultra-thin, inert, transparent coating that meets the challenges of product reliability. Parylene provides useful electrical and dielectric properties, dry film lubricity, biocompatibility and biostability to a wide range of applications. This webinar will offer an opportunity for participants to increase their knowledge of Parylene, learn how they are applied and understand how medical devices and other advanced applications can benefit from their properties.

Date: September 11, 2014
Time: 11:00 AM PT / 2:00 PM ET
Duration: 60 minutes

Sponsored by:

Specialty Coating Systems

Hosted by:

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Connecting Devices within the Medical World

As the Medical Industry becomes more advanced and devices are getting smarter, wireless connectivity has become even more crucial. From consumer medical devices, such as the Fit Bit, to connecting patients with their nurses through wireless electronic monitors, how does your company grow and adapt?

Join us to look at some simple ways to add smart phone or mobile connectivity to your devices, and the pitfalls to look out for along the way.

Date: May 22, 2014
Time: 8:00 AM PT / 11:00 AM ET
Duration: 45 minutes

Sponsored by:

Sparton Corporation

Hosted by:

Watch Today!


12 Techniques to Get Better Fluid Dispensing Control in Today’s Life Sciences Market

Are you fully optimizing your current fluid dispensing process? True precision dispensing creates better process control throughout all assembly areas. From choosing the right disposable components to fully incorporating your process into a complete system, an objective evaluation of your current process can have noteworthy gains. When accurate deposits are consistently dispensed, significant savings are realized. Let us show you how to elevate your process in order to increase productivity while reducing costs.

Date: May 20, 2014
Time: 11:00 AM PT / 2:00 PM ET
Duration: 60 minutes

Sponsored by:

NordsonEFD

Hosted by:

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Human Factors Workflow Mapping Techniques

Whether designing a medical device for an entirely new procedure or improving an instrument for an existing procedure, it is essential to first understand the common practices, expectations, and needs of the various users who will interact with the device.

But what do you do with the mountain of observations and insights that result? How do you communicate key findings and opportunities with team members who did not make it out into the field themselves? Reports and specifications can only do so much. Creating a Workflow Map is a much more effective way of establishing a shared understanding of the design problem within your project team and your organization as a whole.

Date: February 27, 2014
Time: 8:00 AM PT / 11:00 AM ET
Duration: 20 minutes

Sponsored by:

DesignConcepts

Hosted by:

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How the New FDA Guidance on ISO 10993 Could Possibly Affect You

In April of 2013 the FDA released a draft guidance on using ISO 10993 for biocompatibility. This draft is intended to replace the #G95-1 document on the current thinking and application of biocompatibility testing for medical devices. In the webinar we will cover three areas of the new document:

1. Summary of ideas that are currently practices by the FDA but this is the first instance that they are put in writing
2. Concepts that can be used for justifying testing plans, and
3. New ideas that are not current thinking with the FDA that could change how you are testing.

Available On-Demand
Date: August 21, 2013
Duration: 60 minutes

Sponsored by:

Hosted by:

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