{"id":503,"date":"2020-09-19T20:40:56","date_gmt":"2020-09-19T18:40:56","guid":{"rendered":"https:\/\/secutify.com\/risk-assessment-in-mechanical-engineering\/"},"modified":"2020-09-26T13:57:49","modified_gmt":"2020-09-26T11:57:49","slug":"risk-assessment-in-mechanical-engineering","status":"publish","type":"post","link":"https:\/\/secutify.com\/en\/risk-assessment-in-mechanical-engineering\/","title":{"rendered":"Risk assessment in mechanical engineering"},"content":{"rendered":"\t\t
CE marking was introduced by the EU with the aim of reducing technical barriers to trade. In the context of CE marking, this goal is achieved by a harmonization concept of the European Commission, based on the so-called \u201cNew Approach\u201d.<\/p>\n
CE marking is intended to ensure that only safe products find their way onto the European market. Before affixing the CE marking, the manufacturer must carry out a conformity assessment to ensure that the respective product meets the requirements of the relevant EU directives\/regulations. To do this, he must determine the applicable EU directives\/regulations and then assess the conformity of his products with these requirements according to the specifications in the directives\/regulations.<\/p>\n
The basic health and safety requirements contained in the applicable directives are binding for the manufacturer. However, it is possible that the goals set with them cannot be achieved due to the state of the art. In this case, the machine must be designed and constructed as far as possible with these objectives in mind.<\/p>\n
The Machinery Directive 2006\/42\/EC naturally has special significance for machine and plant construction. The Machinery Directive requires that a risk assessment be carried out by the manufacturer of the machine as part of the CE marking.<\/p>\n
The risk assessment is required in order to identify the risks posed by products and, with the aid of risk analysis and risk assessment, to reduce the dangers \u2013 and thus provides the manufacturer with legal certainty if used correctly.<\/p>\n
\nMRL, Annex I, 1st edition: The manufacturer of a machine or his authorised representative must ensure that a risk assessment is carried out to determine the health and safety requirements applicable to the machine. The machine must then be designed and constructed taking into account the results of the risk assessment.<\/p>\n<\/blockquote>\n
In addition to the Machinery Directive, other EU directives and EU regulations also require the preparation of a risk analysis and assessment. Here is an exemplary list:<\/p>\n
\n
- Machinery Directive 2006\/42\/EC<\/li>\n
- Low Voltage Directive 2014\/35\/EU<\/li>\n
- EMC Directive 2014\/30\/EU<\/li>\n
- Radio Equipment Directive 2014\/53\/EU<\/li>\n
- Pressure Equipment Directive 2014\/68\/EU<\/li>\n
- ATEX Directive 2014\/34\/EU<\/li>\n
- Medical Device Directive 93\/42\/EEC or Medical Device Directive (EU) 2017\/745<\/li>\n<\/ul>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\tRisk assessment<\/h2>\n
When a company builds, retrofits or interlinks machines, a systematically structured risk assessment is the most important basis for the safe execution of the product. The risk assessment according to EN ISO 12100 (formerly known as hazard analysis) is therefore the central design element for the development of safe machines according to the Machinery Directive.<\/p>\n
Risk assessment and risk reduction as an iterative process<\/h3>\n
The risk assessment according to EN ISO 12100 essentially follows these 5 steps:<\/p>\n
\u00a0<\/b><\/p>\n
\n
- Determining the limits of the machine
<\/strong>This is where the basic conditions for the use of the machine are defined. What it is used for and by whom, in which context and under which boundary conditions (e.g. climatic, local, temporal)
<\/strong><\/li>\n- Risk analysis<\/strong>
Identification of hazards for all life phases and tasks\/operation modes<\/li>\n- Risk assessment<\/strong>
based on the extent of damage and probability of occurrence<\/li>\n- Risk evaluation<\/b>
the decision whether risk reduction is necessary or not<\/li>\n- Risk reduction<\/b>
Find solutions to reduce or eliminate the risk<\/li>\n<\/ol>\nThese 5-steps have to be passed through iteratively, since the application of protective measures can potentially create additional hazards or increase other risks. Thus, it is necessary to continuously check whether new hazards have arisen.<\/p>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\n\t\t\t\t\t\t\tRisk analysis<\/h2>\n
DETERMINATION OF THE LIMITS OF THE MACHINE OR PLANT<\/h3>\n
When determining the limits of the machine, the aim is to define the framework conditions that apply to the use of the machine and thus to the considerations in the risk assessment. This includes determining the scope of application and the characteristics of the machine: e.g. area of application, space requirements, types of energy, auxiliary and operating materials, waste products, service life.<\/p>\n
EN ISO 12100 divides the determination of the limits for this purpose into<\/p>\n