Scrip
Clinica
RA Medtech
RA Pharma
Scrip Clinical Research
Animal Pharm
Email ID
Password
Forgotten password?
Sign me in automatically next time
Advanced Search
Home
Product Sector
Regulatory Region
Pre-marketing Regulation
Post-marketing Regulation
Healthcare Systems
Legal
Structures
|
HTA
|
Pricing and Reimbursement
|
Policy
|
Insurance
|
Healthcare Systems - Policy
Loading POLICY ....
>> More Policy...
EXPERT VIEW
Assessing the size of the US recall issue
27 April 2011
Ashley Yeo
With the US in mid-regulatory review, stakeholders are keenly pushing for a safer and faster system, but there are different views on how these goals should be achieved. That was shown at a hearing of the US Senate's Special Committee on Aging 1 . ...
LATEST FEATURES
Implementing the New EU Legislation on Advanced Therapy Medicinal Products
24 April 2009
The large number of people who attended the European Medicines Agency ’s first workshop on advanced therapy medicinal products reflects the interest ...
Nanotechnology and the European Product Liability Directive
02 April 2009
A key area for the development of nanotechnology is in medicines and medical devices. The application of nanotechnology to health, sometimes referred ...
Navigating the New EU Rules for Medical Device Software
17 March 2009
Directive 2007/47/EC marks the introduction in the European Union of stricter rules for software used with medical devices 1 . The directive, which ...
>> More Latest Features...
LATEST COUNTRY PROFILES
Trademarks Briefing (Devices) - Luxembourg
08 October 2009
Please give details of the major acts and directives governing trademarks. Trademarks are governed in Luxembourg by the: Benelux Convention on ...
Regulation of Medical Devices Briefing - Spain
08 October 2009
1) Which authority is responsible for overseeing the regulation of medical devices and diagnostics in Spain? Agencia Española del Medicamento, the ...
>> More Latest Country Profiles...
MULTIMEDIA
RAJ Devices News Roundup, 11 December 2009
28 July 2011
About Us
Getting Started
Free Trial
Subscribe
Advertise
Guidelines for Authors
Blog
EVENTS
Overview of ISO 13485:2003, the CMDRs, the MDD, and JPAL
21September 2009
Minneapolis (MN), US
