Top Stories
Why UPNs Make Sense for Medical Devices
Mandating the UPN system would help manufacturers better track their products.
Spotlight: Flow Control
A supplier of sapphire and ruby orifices in sizes ranging from 0.0004 to 0.081 in. has introduced a golden orifice series designed to achieve high repeatable flow accuracy.
Getting From Here to There
How to successfully take a medical device from concept to high-volume manufacturing.
Using Green Technology to Machine Materials
The molecular decomposition process helps manufacturers machine materials more efficiently.
Closed-Loop Micropumps
The small size, low power consumption and attractive price of micropumps make them ideal for use in medical delivery systems.
Damage-Free Alloy Conversion for Medical Components
As suppliers rid themselves of traditional lead solders, how do medical device manufacturers cope with the changes? The answer is very carefully.
Automated quantitative microarray assay platforms
A microarray-based assay platform has been developed for high test throughput, with a fully automated protocol.
Is a Consumer-Directed Strategy Right for Your Technology?
Evaluating the market potential for a new medical technology requires an in-depth understanding of a product's intellectual property, regulatory pathway, clinical application, and reimbursement potential.
MedTech Video Vault
MedTech Video Vault, Canon Communications' new online information resource, allows you access to trade show floors by presenting products and services from medical OEM suppliers at the forefront of medical design engineering. It's like being able to visit the trade show floor from your desktop.Now Playing: View clips from this year's MD&M East and MD&M West shows.
Career Network
Today's Top Jobs
- Associate Director, HEOR, Astellas Pharma US, Inc.
- Center Supervisor, Baxter International, Inc
- Manufacturing Mechanic, sanofi pasteur, Acambis Campus
- Mgr, Clinical Development, Baxter International, Inc
- Process Development Scientist, Talecris Biotherapeutics
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Clinical Studies in Italy
Dr Maria E. Donawa
The requirements for conducting medical device clinical studies in Europe are not identical in all Member States.
Court Case on Patent Delays Holds Appeal for Industry
Jason M. Honeyman and MaryDilys Anderson
A disputed legal ruling gives device companies the chance to extend patent terms, provided they take the proper steps.
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Materials Research Society (MRS) Fall Meeting
Date: 11/30-12/04; Location: Boston, MA -
BIOMEDevice
Date: 12/9-12/10; Location: San Jose, CA -
ISET
Date: 1/17-1/21; Location: Hollywood, FL -
Detecting Fraud and Misconduct in Clinical Trials
Date: 1/21-1/22; Location: Costa Mesa, CA -
BIOMEDevice Europe
Date: 2/1-2/2; Location: Paris, FR -
MD&M West
Date: 2/9-2/11; Location: Anaheim, CA - Advanced Reimbursement Symposium
Date: 3/15-3/16; Location: Chicago, IL - Clinical Trial Design For Medical Devices
Date: 3/15-3/16; Location: Malvern, PA - See All Events
From DeviceTalk:
Proposed Senate Bill Lowers Device TaxThe Senate healthcare bill introduced by Sen. Harry Reid reduced the medical device fee from $38 billion to $20 billion.
From Medtech Pulse:
Nanoparticles Enable Scientists to Connect the Dots inside CellsThe joint NIST/NIAID research team has discovered a method of using quantum dots to illuminate the cellular interior to reveal slow processes.
From medtechinsider:
Medical-Grade Silicone Features Enhanced ProcessabilityA new platinum-grade material will soon be introduced by Primasil Silicones.
From IVDT Insight:
OraSure Settles Patent Suit with InvernessOraSure Technologies Inc. announced the settlement of the patent infringement lawsuit filed against OraSure by Inverness Medical Innovations Inc., Inverness Medical Switzerland GmbH, and Church & Dwight Co.
Tips and Tactics: Preparing for eMDR
This webinar features industry experts who will share their insight on best practices in preparing for eMDR. Speakers from Sparta Systems, a leading enterprise quality management software provider, and Inovis, an Electronic Data Interchange solutions provider, will identify eMDR strategies and explain how to navigate eMDR regulation and plan and develop an effective reporting system.
View Archived Webcast
Handling Device Recalls, Corrections, and Removals
Even with the best preparation, a device can go wrong. Regardless of the reason for remedial field corrections, a conscientious manufacturer should aim to correct the problem to maintain costumer loyalty and satisfaction. An effective strategy is essential to surviving a recall.
View Archived Webcast
Featured White Papers
Tuning ERP and the Supply Chain for Profitable Growth
A close link exists between information technology and an organization's ability to execute business efficiently and effectively.
Gaining Competitive Advantage in a Downsized Economy
Outsourcing advanced development to build company value asset by asset.
Effect of Sterilization on the Mechanical Properties of Silicone Rubbers
Findings on the compatibility of various sterilization mechanisms with different silicone types provide guidance to medical device designers on material selection and sterilization limitations.
"In My Defense Let Me State That the Bed Was Already on Fire When I Climbed Into It"
The purpose of this paper is to present the medical device developer guidelines for complying with the "suggestions" of the CDRH.
