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The Canon Communications family of medical technology publications produce a wide variety of FREE Web events on topics of importance to professionals in the medical device industry and related life sciences areas.
Registration for Canon Webcasts isn't limited to publication subscribers; anyone with an interest in the topic can register and attend free of charge. And attendance is not limited to the initial presentation; interested parties can view the archived Webcast at any time.
The links below can be used to view past events. |
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Building Biomaterials
As a device maker, you've probably been given a specific list of approved biomaterials. But it's not always clear how to use that list to suit your application. Hosted by MD&DI , this FREE Webcast features three industry experts who will explore the current state of biomaterials. They will discuss the requirements for material selection. And if the list of approved biomaterials isn't enough to suit your needs, these experts present options for building biomaterials from the ground up.
Originally Broadcast: 4/16/08
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Tubing: Doing More with Less
Experts forecast that the U.S. market for minimally invasive devices and instruments will balloon to $11 billion by 2011. But, along with the potential for profit, the multi-billion-dollar market is presenting new challenges to the tubing industry as it demands tighter tolerances, thinner walls, biocompatible materials, and greater functionality in a much smaller package.
Originally Broadcast: 4/9/08
Sponsored by: MicroLumen and Zeus
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Developing Biochemicals and Chemical Reagents for Next-Generation Immunoassays
Biochemicals and reagents used in diagnostic tests have changed and improved during the past few years. This Webcast will examine current trends and future developments in biochemicals and reagents used in immunoassays.
Originally Broadcast: 4/3/08
Sponsored by: AbD Serotec and Proliant Health and Biologicals and Invitrogen-Dynal
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How To Implement the New European Vigilance Procedures
A revised medical device guidance document on postmarketing vigilance (MEDDEV 2.12-1 rev 5) was published in April 2007 by the European Commission. This webinar will cover all the major revisions, point by point.
Originally Broadcast: 4/2/08
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Reducing Risk Through Packaging, Part I: Understanding the Nuances of ISO 11607
Members of the Sterilization Packaging Manufacturers Council discuss ISO 11607, Packaging for Terminally Sterilized Medical Devices. Split into two parts, the 2006 revision outlines requirements and responsibilities for designing sterile barrier systems and packaging systems and validating forming, sealing, and assembly processes.
Originally broadcast: 2/12/08
Sponsored by: Alcan Packaging and Beacon Converters and PerfecSeal and Rollprint and TOLAS Healthcare Packaging
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The Medtech Marketplace in 2008
To capitalize on the energy behind industry change, company leaders need to be on top of the latest trends. In this Webcast, industry experts provide insights into the factors driving some of medtech's key sectors in 2008 and beyond.
Originally broadcast: 1/16/08
Sponsored by: Sebra
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