|
How are Safety Instrumented Systems derived? Generally the significant Hazards for a process are identified by the duty holder in a Hazard & Risk Analysis. The method and approach for conducting a HRA is documented in both standards. It is the first stage of the lifecycle as defined in IEC61511. The HRA is used to derive the Safety Requirement Specification.
What is a Safety-Related or Safety Instrumented System (SIS)?
How does product conformance relate to specific Safety Integrity Levels (SILs)?
What are typical applications requiring SIS? |
|
What information should I expect from a supplier of devices or sub-systems? When devices or sub-systems are integrated into a SIS it is necessary to take into account the contribution that these elements will make toward the performance of the system in relation to Safety-Integrity. Specific information relating to design and reliability of these devices or sub-systems is required, this should include some or all of the information summarised below:- - Specification covering functional, interface and environmental aspects. - Estimated failure rate (due to random hardware failure) for each failure mode. - Diagnostic coverage and diagnostic test interval. - Hardware fault tolerance - Information needed to identify hardware and software configuration - Information needed to enable the derivation of the Safe Failure Fraction - Documentary evidence of validation. - Safety Integrity Level capability.
What is the difference between Risk and Safety Integrity? |