PRICES include / exclude VAT
Homepage>BS Standards>11 HEALTH CARE TECHNOLOGY>11.040 Medical equipment>11.040.01 Medical equipment in general>PD IEC/TR 80001-2-2:2012 Application of risk management for IT-networks incorporating medical devices Guidance for the disclosure and communication of medical device security needs, risks and controls
Sponsored link
immediate downloadReleased: 2012-07-10
PD IEC/TR 80001-2-2:2012 Application of risk management for IT-networks incorporating medical devices Guidance for the disclosure and communication of medical device security needs, risks and controls

PD IEC/TR 80001-2-2:2012

Application of risk management for IT-networks incorporating medical devices Guidance for the disclosure and communication of medical device security needs, risks and controls

Format
Availability
Price and currency
English Secure PDF
Immediate download
348.00 EUR
You can read the standard for 1 hour. More information in the category: E-reading
Reading the standard
for 1 hour
34.80 EUR
You can read the standard for 24 hours. More information in the category: E-reading
Reading the standard
for 24 hours
104.40 EUR
English Hardcopy
In stock
348.00 EUR
Standard number:PD IEC/TR 80001-2-2:2012
Pages:58
Released:2012-07-10
ISBN:978 0 580 75100 4
Status:Standard
DESCRIPTION

PD IEC/TR 80001-2-2:2012


This standard PD IEC/TR 80001-2-2:2012 Application of risk management for IT-networks incorporating medical devices is classified in these ICS categories:
  • 11.040.01 Medical equipment in general
IEC/TR 80001-2-2:2012(E), which is a technical report, creates a framework for the disclosure of security-related capabilities and risks necessary for managing the risk in connecting medical devices to IT-networks and for the security dialog that surrounds the IEC 80001-1 risk management of IT-network connection. This security report presents an informative set of common, high-level security-related capabilities useful in understanding the user needs, the type of security controls to be considered and the risks that lead to the controls. Intended use and local factors determine which exact capabilities will be useful in the dialog about risk. The capability descriptions in this report are intended to supply health delivery organizations (HDOs), medical device manufacturers (MDMs), and IT vendors with a basis for discussing risk and their respective roles and responsibilities toward its management. This discussion among the risk partners serves as the basis for one or more responsibility agreements as specified in IEC 80001-1.