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[EU]

Simple smart phones and remote controls help elderly and disabled to manage their homes
2011-01-06

The Osteoporotic Virtual Physiological Human
2011-01-04

Second MedEX Workshop: Call for Paper deadline 01 February 2011
2011-01-04

A new system for event-based surveillance will be presented at CeBIT 2011 and at IMED 2011
2011-01-04

Flanders Primary Care Safe - Market Consultation: deadline 28/01/2011
2011-01-04

INTERSTRESS newsletter
2011-01-04

Medicine: the 3D revolution
2010-12-22

Interreality in the Management and Treatment of Stress-Related Disorders: video
2010-12-22

Towards Effective eHealth Interoperability Certification and Conformance Testing
2010-12-22

ICT Policy Support Programme - 2011 Work Programme and Call for Proposals
2010-12-20

Call For Papers IEEE TBME Letters - Special Issue on Multi-Scale Modeling and Analysis for Computational Biology and Medicine
2010-12-20

Call for papers - special Issue on Medical Imaging in Computational Physiology - IEEE Transactions on Medical Imaging
2010-12-20

Ready to grow? Shaping future EU support for business - Conference on the future of the Competitiveness and Innovation Programme
2010-12-20

Reminder: Augmented Human conference paper submission
2010-12-17

preDiCT: Predicting Drug Cardiac Toxicity
2010-12-17

Commission signs eHealth agreement with US Department of Health
2010-12-17

Plate-forme eHealth Belgique Infoday
2010-12-17

Public consultation on the Raw Materials Initiative
2010-07-12

New references of harmonised standards for Medical Devices in OJ C 183 of 7 July 2010
2010-07-08

New references of harmonised standards for Medical Devices in OJ C 183 of 7 July 2010
2010-07-08

CE marking – what does it really mean?
2010-06-15

CE marking – what does it really mean?
2010-06-15

Regulation amending the REACH Annexes relevant for SDS (safety data sheet)
2010-06-02

Regulation amending the REACH Annexes relevant for SDS (safety data sheet)
2010-06-02

SCENHIR opinion on the safety of reprocessed single-use devices
2010-04-28

SCENHIR opinion on the safety of reprocessed single-use devices
2010-04-28

Review of the European Standardisation System
2010-03-24

Review of the scope of REACH
2010-03-23

Revision of the In vitro diagnostic medical devices Directive
2010-03-22

A mark Europeans can trust
2010-03-10

Radiation Criteria for Acceptability of Medical Radiological Equipment Used in Diagnostic Radiology, Nuclear Medicine and Radiotherapy
2010-02-03

Qualification of hygienic tampons containing lactic acid producing bacteria
2010-02-01

New references of harmonised standards for Medical Devices in OJ C 293 of 2 December 2009
2009-12-07

New references of harmonised standards for Medical Devices in OJ C 293 of 2 December 2009
2009-12-07

Discussion paper on Unique Device Identification - UDI
2009-12-04

The financing of biopharmaceutical product development in Europe
2009-12-01

Call for scientific data on peanut oil and wheat proteins
2009-11-09

European workshops on the disclosure of environmental, social and governance information.
2009-10-15

European workshops on the disclosure of environmental, social and governance information.
2009-10-15

Commission paves the way for vaccinations for influenza pandemic (H1N1) 2009
2009-09-29

Commission paves the way for vaccinations for influenza pandemic (H1N1) 2009
2009-09-29

Guidance on the CLP Regulation published by the European Chemicals Agency (ECHA)
2009-09-03

Guidance on the CLP Regulation published by the European Chemicals Agency (ECHA)
2009-09-03

Assistance to SMEs: Registering trademarks in China
2009-08-31

Assistance to SMEs: Registering trademarks in China
2009-08-31

New Interpretative Documents on the Medical Devices Directives
2009-08-26

New Interpretative Documents on the Medical Devices Directives
2009-08-26

Taking on endless possibilities, € 114 million for space research
2009-07-30

Taking on endless possibilities, € 114 million for space research
2009-07-30

A sharper view of Europe’s enterprise landscape
2009-07-16

Business Panel on future EU innovation policy for open consultation
2009-07-07

New guidance on active implantable medical devices
2009-07-06

New documents on Medical Devices
2009-07-06

New guidance on active implantable medical devices
2009-07-06

New documents on Medical Devices
2009-07-06

Clinical Trials Directive
2009-06-22

The new EU Regulation on classification, labelling and packaging of chemicals based on UN GHS is in force.
2009-02-04

The new EU Regulation on classification, labelling and packaging of chemicals based on UN GHS is in force.
2009-02-04

European Commission proposes new strategy to address EU critical needs for raw materials
2008-11-04

European Commission proposes new strategy to address EU critical needs for raw materials
2008-11-04

Cosmetics safety rules to be rejuvenated
2008-06-03

Simplification of 8 metrology directives
2008-05-23

[IEC]

IEC 60601-2-46 Ed. 2.0
2010-12-16

IEC 60825-2 Consol. Ed. 3.2 (incl. am1+am2)
2010-12-14

IEC 60601-2-4 Ed. 3.0
2010-12-08

Project IEC 60731 Ed. 3.0
2010-12-03

Project IEC 60601-2-23 Ed. 3.0
2010-12-03

Project IEC 60601-2-49 Ed. 2.0
2010-12-03

Project IEC 60601-2-45 Ed. 3.0
2010-11-12

Project IEC 60601-2-57 Ed. 1.0
2010-11-12

IEC 62464-2 Ed. 1.0
2010-11-10

IEC 60601-2-8 Ed. 2.0
2010-11-10

IEC/TR 60825-17 Ed. 1.0
2010-11-10

IEC 80001-1 Ed. 1.0
2010-10-27

IEC 60601-2-52 Ed. 1.0
2010-09-22

IEC 60825-2-am2 Ed. 3.0
2010-09-22

IEC 60601-2-50 Ed. 2.0
2010-08-10

IEC 60601-2-44 Ed. 3.0
2010-05-19

IEC 60601-1-SER Ed. 1.0
2010-04-29

IEC 60601-1-11 Ed. 1.0
2010-04-28

IEC 60526 Ed. 2.0
2010-04-22

IEC 60601-2-43 Ed. 2.0
2010-03-25

IEC 60601-1-2 Ed. 3.0
2010-03-16

IEC 60601-2-54 Ed. 1.0
2010-03-10

IEC 60601-2-28 Ed. 2.0
2010-03-10

IEC 60601-2-33 Ed. 3.0
2010-03-10

IEC 60601-1-6 Ed. 3.0
2010-01-27

IEC 60613 Ed. 3.0
2010-01-27

IEC 80601-2-30 Ed. 1.0
2010-01-14

IEC 60825-1 Ed. 2.0
2009-12-17

IEC 62563-1 Ed. 1.0
2009-12-10

IEC 60601-2-52 Ed. 1.0
2009-12-10

ISO 80601-2-56 Ed. 1.0
2009-12-08

ISO 80601-2-56 Ed. 1.0
2009-12-08

IEC 60825-4 Consol. Ed. 2.1 (incl. am1)
2009-10-28

IEC 80601-2-35 Ed. 2.0
2009-10-20

IEC/TR 62354 Ed. 2.0
2009-10-14

IEC 60789 Ed. 3.0
2009-10-13

IEC 60601-2-1 Ed. 3.0
2009-10-13

IEC/TR 80002-1 Ed. 1.0
2009-09-23

IEC 62083 Ed. 2.0
2009-09-23

IEC 62083 Ed. 2.0
2009-09-23

IEC 60601-2-13 Consol. Ed. 3.1 (incl. am1)
2009-08-31

IEC 60601-2-41 Ed. 2.0
2009-08-12

IEC 60601-2-18 Ed. 3.0
2009-08-12

IEC 60601-2-41 Ed. 2.0
2009-08-12

IEC/TR 62471-2 Ed. 1.0
2009-08-06

IEC 60601-2-5 Ed. 3.0
2009-07-30

IEC 60601-2-54 Ed. 1.0
2009-06-29

IEC 60601-2-54 Ed. 1.0
2009-06-29

IEC 62467-1 Ed. 1.0
2009-06-09

ISO 81060-2 Ed. 1.0
2009-05-08

IEC 60601-2-44 Ed. 3.0
2009-02-25

IEC 60601-2-44 Ed. 3.0
2009-02-25

IEC 60601-1 Ed. 3.0
2009-01-28

IEC 61676 Consol. Ed. 1.1 (incl. am1)
2009-01-26

IEC/TR 62296 Ed. 2.0
2009-01-22

IEC 61676-am1 Ed. 1.0
2008-11-27

IEC 61676-am1 Ed. 1.0
2008-11-27

IEC/TR 60930 Ed. 2.0
2008-09-19

IEC/TR 61258 Ed. 2.0
2008-08-28

IEC 62494-1 Ed. 1.0
2008-08-13

IEC 62494-1 Ed. 1.0
2008-08-13

IEC 60825-1 Ed. 2.0
2008-08-12

[ISO]

ISO/FDIS 10943 - Ophthalmic instruments -- Indirect ophthalmoscopes
2011-01-03

ISO/FDIS 10943 - Ophthalmic instruments -- Indirect ophthalmoscopes
2011-01-03

ISO/PRF TS 19218-1 - Medical devices -- Hierarchical coding structure for adverse events -- Part 1: Event type codes
2011-01-03

ISO/PRF TS 19218-1 - Medical devices -- Hierarchical coding structure for adverse events -- Part 1: Event type codes
2011-01-03

ISO/FDIS 24415-2 - Tips for assistive products for walking -- Requirements and test methods -- Part 2: Durability of tips for crutches
2011-01-03

ISO/FDIS 24415-2 - Tips for assistive products for walking -- Requirements and test methods -- Part 2: Durability of tips for crutches
2011-01-03

ISO/FDIS 24415-2 - Tips for assistive products for walking -- Requirements and test methods -- Part 2: Durability of tips for crutches
2011-01-03

ISO/FDIS 24503 - Ergonomics -- Accessible design --Tactile dots and bars on consumer products
2010-12-30

ISO/FDIS 24503 - Ergonomics -- Accessible design --Tactile dots and bars on consumer products
2010-12-30

ISO/FDIS 24503 - Ergonomics -- Accessible design --Tactile dots and bars on consumer products
2010-12-30

ISO/FDIS 15378 - Primary packaging materials for medicinal products -- Particular requirements for the application of ISO 9001:2000, with reference to Good Manufacturing Practice (GMP)
2010-12-17

ISO/FDIS 15378 - Primary packaging materials for medicinal products -- Particular requirements for the application of ISO 9001:2000, with reference to Good Manufacturing Practice (GMP)
2010-12-17

ISO/FDIS 80601-2-61 - Medical electrical equipment -- Part 2-61: Particular requirements for basic safety and essential performance of pulse oximeter equipment
2010-12-16

ISO/FDIS 23409 - Male condoms -- Requirements and test methods for condoms made from synthetic materials
2010-12-16

ISO/FDIS 11156 - Packaging -- Accessible design -- General requirements
2010-12-15

ISO/FDIS 11156 - Packaging -- Accessible design -- General requirements
2010-12-15

ISO/FDIS 11156 - Packaging -- Accessible design -- General requirements
2010-12-15

ISO/PRF TS 11942 - Dentistry -- Standards development vocabulary
2010-12-14

ISO/PRF TS 11942 - Dentistry -- Standards development vocabulary
2010-12-14

ISO 27020:2010 - Dentistry -- Brackets and tubes for use in orthodontics
2010-12-13

ISO/FDIS 18192-1 - Implants for surgery -- Wear of total intervertebral spinal disc prostheses -- Part 1: Loading and displacement parameters for wear testing and corresponding environmental conditions for test
2010-12-10

ISO 80369-1:2010 - Small-bore connectors for liquids and gases in healthcare applications -- Part 1: General requirements
2010-12-08

ISO 80369-1:2010 - Small-bore connectors for liquids and gases in healthcare applications -- Part 1: General requirements
2010-12-08

ISO 24501:2010 - Ergonomics -- Accessible design -- Sound pressure levels of auditory signals for consumer products
2010-12-03

ISO 24501:2010 - Ergonomics -- Accessible design -- Sound pressure levels of auditory signals for consumer products
2010-12-03

ISO/FDIS 3107 - Dentistry -- Zinc oxide/eugenol cements and zinc oxide/non-eugenol cements
2010-12-02

ISO 24502:2010 - Ergonomics -- Accessible design -- Specification of age-related luminance contrast for coloured light
2010-12-02

ISO 24502:2010 - Ergonomics -- Accessible design -- Specification of age-related luminance contrast for coloured light
2010-12-02

ISO 24502:2010 - Ergonomics -- Accessible design -- Specification of age-related luminance contrast for coloured light
2010-12-02

ISO/FDIS 10271 - Dentistry -- Corrosion test methods for metallic materials
2010-12-01

ISO 21671:2006/FDAmd 1
2010-12-01

ISO/FDIS 17853 - Wear of implant materials -- Polymer and metal wear particles -- Isolation and characterization
2010-11-30

ISO/FDIS 13132 - Laboratory glassware -- Petri dishes
2010-11-29

ISO/FDIS 13130 - Laboratory glassware -- Desiccators
2010-11-29

ISO/FDIS 13079 - Laboratory glass and plastics ware -- Tubes for the measurement of the erythrocyte sedimentation rate by the Westergren method
2010-11-29

ISO/FDIS 11040-2 - Prefilled syringes -- Part 2: Plunger stoppers for dental local anaesthetic cartridges
2010-11-26

ISO/FDIS 11040-2 - Prefilled syringes -- Part 2: Plunger stoppers for dental local anaesthetic cartridges
2010-11-26

ISO/FDIS 13926-2 - Pen systems -- Part 2: Plungers stoppers for pen-injectors for medical use
2010-11-26

ISO/FDIS 11040-2 - Prefilled syringes -- Part 2: Plunger stoppers for dental local anaesthetic cartridges
2010-11-26

ISO 29941:2010 - Condoms -- Determination of nitrosamines migrating from natural rubber latex condoms
2010-11-25

ISO/FDIS 11990-1 - Lasers and laser-related equipment -- Determination of laser resistance of tracheal tubes -- Part 1: Tracheal tube shaft
2010-11-24

ISO 14155 - Clinical investigation of medical devices for human subjects -- Good clinical practice
2010-11-17

ISO/FDIS 23500 - Guidance for the preparation and quality management of fluids for haemodialysis and related therapies
2010-11-16

ISO/TR 22442-4:2010 - Medical devices utilizing animal tissues and their derivatives -- Part 4: Principles for elimination and/or inactivation of transmissible spongiform encephalopathy (TSE) agents and validation assays for those processes
2010-11-16

ISO/PRF TR 28642 - Dentistry -- Guidance on colour measurement
2010-11-15

ISO/FDIS 15621 - Urine-absorbing aids -- General guidelines on evaluation
2010-11-12

ISO/FDIS 15621 - Urine-absorbing aids -- General guidelines on evaluation
2010-11-12

ISO/FDIS 15621 - Urine-absorbing aids -- General guidelines on evaluation
2010-11-12

ISO/FDIS 8624 - Ophthalmic optics -- Spectacle frames -- Measuring system and terminology
2010-11-04

ISO/FDIS 80601-2-12 - Medical electrical equipment -- Part 2-12: Particular requirements for basic safety and essential performance of critical care ventilators
2010-11-04

ISO 16037:2002/FDAmd 1
2010-11-04

ISO 11979-8:2006/FDAmd 1
2010-11-01

IEC 80001-1:2010 - Application of risk management for IT-networks incorporating medical devices -- Part 1: Roles, responsibilities and activities
2010-10-28

ISO 11986:2010 - Ophthalmic optics -- Contact lenses and contact lens care products -- Determination of preservative uptake and release
2010-10-21

ISO/FDIS 13212 - Ophthalmic optics -- Contact lens care products -- Guidelines for determination of shelf-life
2010-10-01

ISO 9187-2:2010 - Injection equipment for medical use -- Part 2: One-point-cut (OPC) ampoules
2010-09-30

ISO 9187-1:2010 - Injection equipment for medical use -- Part 1: Ampoules for injectables
2010-09-30

ISO 8835-3:2007/Amd 1:2010
2010-09-29

ISO/FDIS 25841 - Female condoms -- Requirements and test methods
2010-09-28

ISO/FDIS 29942 - Prophylactic dams -- Requirements and test methods
2010-09-28

ISO 14729:2001/Amd 1:2010
2010-09-24

IEC 60601-2-52:2009/Cor 1:2010
2010-09-23