Safety requirement specification documentations

Safety Requirements Specification The instrumentation and electrical (I E) requirements are developed to meet the intent of any H RA findings and the process requirements. The design documentation should establish a clear connection between each process hazard and the design of its SIFs. I E personnel should meet with the process engineering representative responsible for the process requirements to ensure that the intent is understood. 

The SIS safety requirements specification may be a single document or a collection of several documents including procedures, drawings or corporate standard practices. These requirements may be developed by the Hazard and Risk Assessment team and/or the project team itself. 

The detailed functional safety requirements specification should include all necessary functions during all modes of operation of the process being protected. Additionally, the periodic testing of all the safety instrumented functions should be provided. This typically requires the definition of maintenance override capabilities so the sensors and final elements can be tested without shutting down the process. The same methodology described in the paragraph above can be used to document these requirements. 

Components and devices used in SIF applications that comply with this standard should be provided with documentation that details all known aspects of installation, maintenance, configuration, programming and operation that should be observed if the component or device is to meet the safety requirements specification of the application. 

Step 5 - Documentation Summarize the findings of the LOPA study and, if appropriate, document that the proposed change meets the corporate risk tolerance criteria/local code targets. Safety Requirements Specification (SRS) is defined to undertake appropriate cost-effective designs for SISs in order to achieve optimal test and maintenance strategies for the lifespan of the plant... 

Each safety instrumented function is documented in the safety requirements specification. That document (or collection of documents) includes all functional information, logic, performance information, timing, b q)ass/maintenance requirements, reset requirements, the safety integrity level for each safety instrumented function, and any other requirement information that the designers may need. 

The conceptual design process for a safety instrumented function begins with a Safety Requirements Specification (SRS). The SRS is an important document. It should contain complete specifications for designing all the safety instrumented functions. For each SIF the following information should be included ... 

Solution For each piece of equipment related to the safety instrumented function, one must ask if that equipment is needed to protect against the specified hazard. In this SIF, the hand-switch was added only to meet local regulatory requirements and is not part of the automatic protection so it is excluded. The pump is turned off to protect it from overload so it is not part of this SIF. The inlet valve for the other unit does not have to close to protect against this hazard so it is excluded. Although the need for the inlet valve closure is debatable, it does help reduce downstream pressure and was therefore included in the SIF. The SIF primary equipment is the LT-2025 level sensor, the VI-2002 Inlet Valve and the VI-2003 Outlet Valve. This is marked in the cause and effect diagram with an X. Other equipment is auxiliary. It is marked in the cause and effect diagram with an A. This information must be documented in the Safety Requirements Specification (SRS). 

Prior to carrying out SIL verification calculations for Safety Instrumented Functions (SIF) it is essential and very important that each function and its associated input and output signals be weU defined. The identification of the SIF is part of the analysis phase and the detail requirements for each function are documented in the Safety Requirements Specifications (SRS). 

This software safety requirements specification is the softwcffe design prime specification document for the SRECS, and would be the document that the software validation will be made against cifter the softwcue design and verification analysis cuid tests are done. 

SIS safety requirements specification (SRS) To specify the requirements for each SIS, in terms of the required safety instrumented functions and their associated safety integrity, in order to achieve the required functional safety. 10 No specific guidance on documenting the SRS. An example is shown in ISA-TR84.00.04 Part 2. All three technical reports (ISA-TR84.00.02, 03, and 04) provide fundamental considerations for SRS development. 

Figure G.1 illustrates the primary and secondary concerns of each failure classification and how they affect the plant operation. The Probability to Fail on Demand Dangerous Undetected (PFDDU) is related to the Safety Integrity Level, which is defined by the H RA findings and documented in the safety requirements specification.

To determine the required fault tolerance for PE logic solvers, the SIL of the SIF and the SFF of the PE logic solver should be determined. The SIL Is documented in the Safety Requirement Specification. The SFF of the PE logic solver is typically determined by a failure mode and effect analysis (FMEA) and is often supplied by the manufacturer for the specific version being specified. 

What is the hazard This should be documented in the hazard and risk analysis and in the safety requirements specification. Care should be taken to ensure that the hazard is fully understood. 

While the requirement in Clause 11.2.8 allows you to specify an alternate way to provide this protection in your Safety Requirements Specification, just stating that you will not provide it is not an acceptable alternative. Refer to Annex B of this technical report for a discussion of operator-initiated safety functions and to Annex F for a discussion of the relationship between the SIS and BPCS. Any procedures required to continue safe operation should be documented, including the training of operation and maintenance personnel. 

In accordance with lEC 61508/61511, the overall required safety management and proper technical activities relates with all documentation for SIS are summarized in safety life cycle. The purpose of analysis phase is to identify hazards and assess safety requirements of SIS. Safety Requirements Specification (SRS) of SIS should contain critical information which includes functional description... 

For example, the equipment tags of the Safety Instrumented Systems (SIS) should be specified in the Safety Requirement Specification (SRS), a live document made specifically for every installation (GL-070 2004 IEC 61508 2010). The PS should contain links to such relevant documentation. In addition to specific requirements for safety critical and barrier functions, the PS should have a clear description of equipment groups that are considered as part of the SCS/SBS. A properly created PS will allow the correct identification of critical equipment tags and the implementation of data into the CMMS. 

The problem for the safety life cycle team is that each new safety measure may require an update to the documentation already drafted for the safety requirements specifications. 

Using the above requirements the completed allocation phase will provide a well-documented baseline for the completion of the detailed safety requirements specification for the SIS. The safety integrity requirements for the SIS are then developed to conform to the following requirements summarized from phase 9. 

We have seen how the safety requirement specification has been expanded from overall safety requirements through allocation into a detailed SRS for the safety instrumented system. The result of these activities will be a fully documented record of the design requirements and the history of where the requirements have come from. 

Task detail 1) Provide a conceptual design for a safety trip system that will protect the plant against defined risks during normal operation and during start up. 2) Define the functional requirements in a logic diagram suitable for documenting into a safety requirements specification. 

Many rubber products, when exported to the member states of the European Union, must comply with the requirements of the relevant legislation approach. The EU Directives of New Approach and Directives of Sectoral Approach are legislative provisions that must especially be followed. Directives of New Approach confine the requirements to the protection of health, property and environment and the safety requirements. The Directives of New Approach lay down the uniform procedure of approval of conformity. Harmonised European standards, giving detailed specifications of the product, follow these Directives. Detailed requirements are given in the Directives of Sectoral Approach and they have to be interpreted individually. The essential concepts are explained and a review of the most important documents is presented. 

Each phase of the SLC must be controlled to maximize the probability that a finished system meets all quality, regulatory, safety, and specification requirements. If an SLC approach is applied properly, no additional work will be required to validate a system. For each SLC period and event, computer systems validation requires that the development processes are documented work products. As explained in Chapter 2, phase gate verification activities performed during each event may be a perfect place to review and quantify the quality of all products needed to support the next phase. 

Gather the requirements for the systems including functional (e.g. operational checks) requirements, nonfunctional (e.g., coding standards) requirements, users, company-wide regulatory compliance (e.g., Part 11 technical control), safety, process, and other applicable requirements Characterize information, assess its value to the organization, and incorporate information quality as part of the project plan Conduct a system (hardware, software, and process) risk analysis. New requirements may be found as the result of the risk analysis. Any new requirements must be documented in the requirements specification deliverable... 

Formal reviews normally require appropriate documentation. For example. Excel spreadsheets or Word templates are available for conducting safety reviews to ensure that a specific process has been used in the analysis and to document the results of the review. The documentation should include the team members, the dates and times of the review, the functional area of each team member, the purpose of the review, the equipment and processes being analyzed, key specifications for the equipment (e.g., maximum flow rate), what codes and standards apply to the review if any, and a discussion of past incidents that may be relevant to what is being reviewed. The review should consider the equipment and materials in the vicinity of what is being reviewed. For example, fuel storage tanks or high voltage electrical equipment in... 

Job description and person specification documents that contain safety information can clearly provide the foimdation for the development of a recruitment and selection program which has at least the possibility of a successful outcome. Further, Thompson and Thompson (1982) provide an excellent review of the steps required to help ensure that courts accept job analysis information as the foundation of selection predictor development and or selection decisions. Furthermore, a job description that includes a section on safety can be used in the expectation setting processes as discussed in Chap. 3, Sect. 3.7.2. In contrast, if there has been no systematic attempt to understand what the requirements are to perform a job in a safe manner, it is unlikely that the recruitment and selection system will be delivering the safety benefits that it potentially could. Furthermore, it is likely that employees trust in these processes to deliver a safe new employee may be somewhat misplaced. 

For each phase, design documents of safety systems, based on SRP BTP-14, of the software development life cycle, include software plans, software requirement specification, software design output, source code listing, and test reports. These documents are subject to the IV V review. 

Suppliers and generators of hazardous materials used in the workplace are required to document the specific hazards and related safety precautions and procedures. To do this, they generally create MSDSs. An MSDS contains information about chemical properties, health and physical hazards, first aid and medical treatment, emergency response, and the handling and disposal of chemicals. The MSDS should be concise, and immediately accessible and usable. MSDSs are available for chemical products from all U.S. and most European suppliers or manufacmrers. 

Having standards for each element of the safety system means that safety issues are documented and the requirements are clearly spelled out. Both managers and employees prefer safety directives and policies in writing so that expectations at all levels are clearly spelled out. Safety standards commit the organization and its members to carry out certain safety activities on a regular basis, and who must perform the activity and what the required result is are clearly laid out in the standard. Having committed the organization and its members to specific standards creates the foundation of the company s safety culture—its safety personality. 

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