functional safety of medical devices

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Your challenges Medical devices are among the most highly regulated products in the world today. A single functional failure can mean the difference between life and death for patients. The World Health Organisation has recommended that governments worldwide make national regulations for medical devices an integral part of their overall national health systems. What is functional safety in medical devices? Traditional safety assessment focuses on potential hazards from electrical, mechanical or other aspects of a design occurring during usage. Functional safety is an additional step focussing on the reliability of the product to function correctly and safely in response to its inputs. It provides assurance that safety-related systems in the device will offer the necessary risk reduction required to minimise the severity and probability of harm in the event of malfunction. Why is functional safety important for your business? Ensuring the functional safety of medical devices is critically important for manufacturers, importers and resellers, as these devices can impact the health and wellbeing of the operators and patients that use them. By undertaking risk analysis and manufacturing medical devices that are functionally safe, your company benefits from increased market acceptance and positive brand associations. Failure to ensure functional safety can have dire consequences. Functional safety expertise from TÜV SÜD Having developed the first functional safety certification programme for professionals in the process industry over 10 years ago, TÜV SÜD is a pioneer in functional safety services. We are one of the few third-party conformity assessment bodies with functional safety experts for medical devices who can provide functional safety tests throughout your product development cycle – from concept to final production. TÜV SÜD Product Service Functional safety for medical devices Assuring the safety and reliability of high-risk medical devices. Choose certainty. Add value.

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Page 1: Functional Safety of Medical Devices

Your challengesMedical devices are among the most highly regulated products in the world today. A single functional failure can mean the difference between life and death for patients. The World Health Organisation has recommended that governments worldwide make national regulations for medical devices an integral part of their overall national health systems.

What is functional safety in medical devices?Traditional safety assessment focuses on potential hazards from electrical, mechanical or other aspects of a design occurring during usage. Functional safety is an additional step focussing on the reliability of the product to function correctly and safely in response to its inputs. It provides assurance that safety-related systems in the device will offer the necessary risk reduction required to minimise the severity and probability of harm in the event of malfunction.

Why is functional safety important for your business?Ensuring the functional safety of medical devices is critically important for manufacturers, importers and resellers, as these devices can impact the health and wellbeing of the operators and patients that use them. By undertaking risk analysis and manufacturing medical devices that are functionally safe, your company benefits from increased market acceptance and positive brand associations. Failure to ensure functional safety can have dire consequences.

Functional safety expertise from TÜV SÜDHaving developed the first functional safety certification programme for professionals in the process industry over 10 years ago, TÜV SÜD is a pioneer in functional safety services. We are one of the few third-party conformity assessment bodies with functional safety experts for medical devices who can provide functional safety tests throughout your product development cycle – from concept to final production.

TÜV SÜD Product Service

Functional safety for medical devicesAssuring the safety and reliability of high-risk medical devices.

Choose certainty.Add value.

Page 2: Functional Safety of Medical Devices

Our functional safety testing assessment services Functional safety should be addressed throughout the product development cycle, particularly in the product’s initial design, to avoid costly rework. Our testing services cover every step of product development.

Independent safety assessment (ISA)TÜV SÜD’s team of experts can test the functional safety concept of a medical device while it is in the design stage, and after it is implemented and prototyped. We also offer ISA on the overall risk management system to determine if it is sufficient for the stringent requirements placed on medical devices.

Software safety assessmentA software glitch in sophisticated medical equipment such as MRI and X-Ray machines can have catastrophic consequences for patients and operators. That is why TÜV SÜD’s functional safety programme emphasises the assessment of medical software against safety standards such as IEC 60601 and IEC 62304.

Product testingWe also offer electrical safety testing, electromagnetic compatibility testing and environmental testing services for medical devices.

Your business benefits

Cultivate a trusted brand – built upon a line of products known to be functionally safe with fewer incident reports.

Reduce cost and time – by minimising corrective actions in the field as well the costs of re-engineering products with poor functional safety.

Gain a competitive edge – by working with our diverse and industry-leading experts, who will provide you with the highest quality reports, keeping you one step ahead of the competition.

Why choose TÜV SÜD?TÜV SÜD developed the world’s first functional safety certification programme for professionals in the process industry in 1999. Since then, we have certified more than 1,000 functional safety experts globally and issued more than 2,000 certificates for functionally safety tested products. Our experts preside on standardisation committees for functional safety and can inform you about emerging standards and regulations so that you stay ahead of the competition.

In the field of medical devices, TÜV SÜD is the largest Notified Body in the world, having over 400 dedicated medical health and services experts situated in major markets worldwide. In addition, we have a dedicated Regulatory Foreign Affairs & Clinical Department for monitoring and understanding updates in medical health services and devices regulations worldwide.

Choose certainty. Add value.TÜV SÜD is a premium quality and safety solutions provider that specialises in testing, inspection, auditing and certification. Represented in over 800 locations worldwide, we hold accreditations in Europe, the Americas, the Middle East and Asia. By delivering objective service solutions to our customers across their entire supply chain, we add tangible value to business and the environment.

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Related services

TÜV SÜD provides the following related services: Assessments of clinical evaluations Electrical, mechanical and software safety Expertise in high-risk medical devicesIEC 60601-1:2005 (3rd Edition)

TÜV SÜD Product Service Octagon House, Concorde Way, Segensworth North, Fareham, Hampshire, PO15 5RL+44 (0)1489 558100 [email protected] www.tuv-sud.co.uk