Your Monthly Download List

Don't miss these technical resources on packaging, tubing, biocompatibility, and more.

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We've put together a list of the latest how-to medtech webcasts and whitepapers available on Qmed. You’ll find expertise on everything from design and business advice to materials and adhesives to manufacturing, packaging, and outsourcing. Click on any of the links below to download a paper or register for a Webinar.

We’ll be sharing new additions every month. We’ll also share news on upcoming educational offerings at upcoming MD&M and BIOMEDevice events.

And if you’re looking for education on a topic you don’t see, please feel free to let us know at daphne.al[email protected]. We welcome suggestions from our medtech community.

Webcasts:

Packaging Validation of Medical Devices – Impact of the Revisions of ISO 11607 and Suitable Strategies

Should you prepare for changes to packaging and testing requirements? Listen to this webinar for an overview of different testing standards, the current status and expectations of FDA, and a discussion on the upcoming revision of international standard ISO 11607-1 and -2.

Disinfectant-Resistant Polymers for Medical Equipment Housings
Ensure proper material selection for medical equipment housings by taking into account the increased use of disinfectants to prevent hospital-acquired infections (HAIs). Learn how to select polymers that prevent stress cracking and compare your options based on retention of mechanical properties.

Focus on Fundamentals 3-Day Course now available on demand
Day 1: What is Changing in the Global Regulatory Landscape
Keep your biocompatibility program current by reviewing changes in regulatory standards, including ISO 10993, medical device regulations, and FDA guidance. 

Day 2: Chemical Characterization and Toxicological Risk Assessment for Medical Device Biocompatibility
Understand how chemical characterization per ISO 10993-18 can be used to support biocompatibility of medical devices.  has become a common occurrence. Learn how results are used within a toxicological risk assessment per ISO 10993-17.

Day 3: How to Address Regulatory Change in Your Current Biocompatibility Program
Learn how to evaluate your biocompatibility information and determine what the gaps are and your options in addressing them.

 

Whitepapers:

Design and Scale Shaped Liquid Tight Bags without the Risks
Learn how polyolefins—instead of PVC—could be used for soft, flexible, liquid-tight medical bags with shapes and fitments

Product Centric QMS: A Critical Advantage for Regulated Companies
Learn how a single, unified quality management system (QMS) can be used to manage medtech documents, SOPs, training records, and quality processes. Read on to learn how a product-centric QMS could help speed product launches and reduce compliance risks.

Top Five Design Mistakes to Avoid When Specifying Stainless Steel Tubing
Avoid common mistakes when specifying tubing, such as forgetting the tubing’s fit with other components or ignoring the surface of the ID. 

Don't Miss These Upcoming Events:

BIOMEDevice San Jose
Connecting Silicon Valley’s brightest medtech professionals and latest medical device technologies
December 5-6, 2018

MD&M West
Anaheim, CA
North America's Largest Annual Medtech Event
February 5-7, 2019

Daphne Allen

Daphne Allen is editor-in-chief of MD+DI. She previously served as executive editor of Pharmaceutical & Medical Packaging News, which serves as the pharmaceutical and medical device channel of Packaging Digest. Daphne has covered medical device packaging, labeling, manufacturing, and regulatory issues as well as pharmaceutical packaging for more than 20 years. She is also a member of the Institute of Packaging Professionals's Medical Device Packaging Technical Committee. Follow her on Twitter at @daphneallen.

 

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