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En Iso 14971 2012

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The document discusses whether Content Deviation #3 of ISO 14971 is aligned with the EU regulatory framework regarding consideration of economic factors in risk management.

The document argues that removing economic considerations from risk management is not aligned with the legislative intent of the EU Medical Devices Directive as specified in recitals, which state that risk reduction must account for technical and economic factors.

The document references a 2007 European Court of Justice decision regarding use of the ALARP ('As Low As Reasonably Practicable') principle, which found its use to be aligned with EU directives.

Kanwal Jit Singh

EN ISO 14971:2012 Content Deviation # 3 IS IT IN TUNE WITH EU REGULATORY FRAMEWORK

Content Deviation # 3 reads as follows Risk reduction "as far as possible" versus "as low as reasonably practicable": a) Annex D.8 to ISO 14971, referred to in 3.4, contains the concept of reducing risks "as low as reasonably practicable" (ALARP concept). The ALARP concept contains an element of economic consideration. However, the first indent of Section 2 of Annex I to Directive 93/42/EEC and various particular. Essential Requirements require risks to be reduced "as far as possible" without there being room for economic considerations. Accordingly, manufacturers and Notified Bodies may not apply the ALARP concept with regard to economic considerations

b)

c)

Section 2 of Annex 1 to MDD read as follows 2. The solutions adopted by the manufacturer for the design and construction of the devices must conform to safety principles, taking account of the generally acknowledged state of the art. In selecting the most appropriate solutions, the manufacturer must apply the following principles in the following order: eliminate or reduce risks as far as possible (inherently safe design and construction), where appropriate take adequate protection measures including alarms if necessary, in relation to risks that cannot be eliminated, inform users of the residual risks due to any shortcomings of the protection measures adopted.

ASPECT 1: CD$# 3 not in tune with the EU Legislative Requirements. The content deviation has interpreted that the as far as possible in the first indent of Section 2 of Annex 1 implies the absence of economic considerations. This blog examines this premise with reference to the legal interpretations available today of the EU Regulatory Framework. The version of the directive

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Bringing fresh insights to add economic value by asking the right questions

Kanwal Jit Singh


that is being referred to in this blog is 1993L0042 EN 11.10.2007 005.001

1.

On Page 3 of the directive the first recital originating on the page reads as Whereas the essential requirements and other requirements set out in the Annexes to this Directive, including any reference to minimizing or reducing risk must be interpreted and applied in such a way as to take account of technology and practice existing at the time of design and of technical and economical considerations compatible with a high level of protection of health and safety; This recital clearly states that the reduction in the risks must be interpreted and applied in such a way to a. Take into account Technology and practices existing at the time of design of the device b. Take into account Technical and Economical Considerations compatible with a high level of protection and safety Therefore there is a clear conflict between the text of the CD# 3 and the text in the recital. The legislative value of a recital has been defined by the Joint Practice Guide: Guide of the European Parliament, the Council and the Commission for persons involved in the drafting of legislation within the Community Institutions. a. In terms of Part 10 of the Guide i. The purpose of the recitals is to set out concise reasons for the chief provisions of the enacting terms, without reproducing or paraphrasing them. They shall not contain normative provisions or political exhortations. The recitals are the part of the act which contains the statement of reasons for the act; They are placed between the citations and the enacting terms. Regulations, directives and decisions must state the reasons on which they are based.

2.

3. 4.

ii. iii. iv.

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Bringing fresh insights to add economic value by asking the right questions

Kanwal Jit Singh


v. The purpose is to enable any person concerned to ascertain the circumstances in which the enacting institution exercised its powers as regards the act in question. This would provide the parties to the dispute the opportunity to defend their interests and to enable the Community judicature to exercise its power of review. The text of the relevant part of the Guide is available at http://goo.gl/iUZ5qV

vi.

vii. 5.

Thus the removal of economic considerations from the risk management process is not in tune with the legislative intent of the directive.

ASPECT 2: JUDICIAL DECISION ON ALARP Item 3 of CD# 3 prohibits the use of ALARP by NBs in the assessment of the Risk Management undertaken by manufacturers. In this context, attention of the standard formulators is drawn to the decision of European Court of Justice in case no. C 127/05 [Commission vs. UK] decided on June 14, 2007. The matter under consideration before the court was
Commission of the European Communities seeks a declaration from the Court that, by restricting the duty upon employers to ensure the safety and health of workers in all aspects related to work to a duty to do this only so far as is reasonably practicable', the United Kingdom of Great Britain and Northern Ireland has failed to fulfil its obligations under Article 5(1) and (4) of Council Directive 89/391/EEC of 12 June 1989 on the introduction of measures to encourage improvements in the safety and health of workers at work

The Commission pleaded that


'... the improvement of workers' safety, hygiene and health at work is an

objective which considerations

should

not

be

subordinated

to

purely

economic

The plea of the Commission was the same as that stated in the justification for the removal of ALARP and economic considerations from the Risk Management Process by the manufacturers and Notified Bodies.

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Bringing fresh insights to add economic value by asking the right questions

Kanwal Jit Singh


The Court decided in declaring that the term SAFAIRP (so far as is reasonably practicable) is in tune with the requirements of the Directive 89/331/EEC and dismissed the action desired by the Commission. IN this context, it is pertinent to invite attention to Paragraphs 34 and 35 of the Opinion given by the Advocate General Mengozzi delivered on January 18, 2007. The Judgment and Opinion can be accessed at http://goo.gl/OiTk0w and http://goo.gl/4nqzdb respectively.

CONCLUSION I therefore urge the powers that be within the EU to recognize the issues in the standard and take appropriate action to remove this from the Annexes in the standard.

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Bringing fresh insights to add economic value by asking the right questions

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