IHS Inc. The Source for Critical Information and Insight
Electronics |  Change

Advanced Search
 
 

EU DIR - European Directives


The Medical Devices industry covers over 8,000 types of products, ranging from simple bandages and spectacles, through life maintaining implantable devices, equipment to screen and diagnose disease and health conditions, to the most sophisticated diagnostic imaging and minimal invasive surgery equipment. The IHS Medical Devices Standards Collections were designed to ensure compliance to the EU Directives that define the “essential requirements” (e.g., protection of health and safety) that goods must meet when they are placed on the EU market.


EU Collections:

Online Access - Subscribers get secure online access to search, view, bookmark, track, and print documents according to the license agreement. Online documents are updated daily. Multiple users can share a single license. You also get access to IHS Standards bibliographic data – more than 1 Million documents.

Individual Documents - IHS sell individual documents through the IHS Store in electronic or hard copy formats. Statistics show that 1 out of every 5 people who purchase individual documents would benefit from an online subscription.  You should consider a collection over individual document purchases if your company buys more than $3,000 in standards per year.


Collection Pricing

Collections are available through online subscription. To speak with an expert about pricing that fits your needs, please complete this form.


Single Document Pricing

Document price is based on page count and publisher. Enter document information in the Standards Store search to the left or call an IHS Subject Matter Expert at 1-888-752-0334.


Request Collections Quote

Choose from the list of collections below, then enter the required information for a quote.

EU DIR - European Directives Collection - Complete

ELECTROMAGNETIC COMPATIBILITY (EU DIR 89/336/EEC)

ELECTROMAGNETIC COMPATIBILITY (EU DIR 89/336/EEC)- BSI/CEN/CENELEC

ELECTROMAGNETIC COMPATIBILITY (EU DIR 89/336/EEC)- ETSI

LOW VOLTAGE EQUIPMENT (Medical) (EU DIR 73/23/EEC)

LOW VOLTAGE EQUIPMENT (Non-Medical) (EU DIR 73/23/EEC)

MEDICAL DEVICES: Active Implantable(EU DIR 90/385/EEC)

MEDICAL DEVICES: General (EU DIR 93/42/EEC)

MEDICAL DEVICES: In Vitro Diagnostic (EU DIR 98/79/EC)

To speak with an IHS Subject Matter Expert call 1-888-752-0334, outside the US/Canada call 303-397-2892.

First Name:

Last Name:

Email address:


ELECTRONICS & TELECOM ENGINEERING STANDARDS NEWS
October 15, 2008
FAQ on EC's Recommendation for Changes in Telecoms Article 7 Rules
On Oct. 15, the European Commission (EC) adopted a new recommendation on procedural rules for the European Union (EU) consultation mechanism, ... more
October 15, 2008
ATIS, IHS Forge Sales Relationship for Telecom, Information, Entertainment Standards, Regulations & Documents
Technical and operations standards from the ATIS will be included in subscription offerings from IHS Inc. ... more
October 15, 2008
Gartner: Worldwide Semiconductor Capital Equipment Spending to Decline 26% in 2008
A collapse in memory spending, combined with a weak economy, is driving a contraction in semiconductor capital equipment spending in 2008, according ... more
October 14, 2008
FAQ on EC's Proposed Revisions to E-Money Directive
This document answers frequently asked questions about the Oct. 13 proposal by the European Commission (EC) to revise current rules governing ... more
October 14, 2008
TIA Recommends FCC Ensure Rules Allow Advanced Cordless Phones to Operate
The Telecommunications Industry Association (TIA) requested the U.S. Federal Communications Commission (FCC) amend frequency rules so that advanced ... more
Show All..