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This Week in Quality Digest Live
FDA Compliance Features
Steven Brand
A crucial method for differentiation (and profitability) in a tight market
Peter Rose
A tardy response will be costly and painful
Stephen McCarthy
Data-driven decisions are only as good as the data that drive them
Jennifer Lopez
How manufacturers can best prepare as the FDA moves to adopt ISO 13485:2016
Stephanie McArdle
The agency seeks to balance expedient exemptions against public transparency about medical devices

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FDA Compliance News
Creates adaptive system for managing product development and post-market quality for devices with software elements
VQIP allows for expedited review and importation for approved applicants that demonstrate safe supply chains
An invite from Alcon Laboratories
Intended to harmonize domestic and international requirements
The FDA wants medical device manufactures to succeed, new technologies in supply chain managment
Pharma quality teams will have performance-oriented objectives as well as regulatory compliance goals
Strategic investment positions EtQ to accelerate innovation efforts and growth strategy
The FDA’s RMAT designation goes live

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Special Report: Hazardous Substance Process Management—Part 1

Video Information

This is Part 1 of our series on hazardous substance process management.

 

In this episode we cover:

* The problem of e-waste shipped overseas

* ROHS

* ROHS-type legislation in the United States

* Dumping non-ROHS compliant electronics in the United States

* Difficulties of meeting ROHS-type legislation

* How a new specification IECQ HSPM QC 080000 can help companies meet the requirements of ROHS and other hazardous substance legislation.

 

For more information and a free white paper on QC 080000 click here.

 

Don't miss the other episodes of this series:

 

Special Report: Hazardous Substance Process Management—Intro

Special Report: Hazardous Substance Process Management—Part 1

Special Report: Hazardous Substance Process Management—Part 2

 
 

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