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SRPS EN ISO 13485:2017

Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)

Nov 30, 2017
Nov 30, 2017

General information

60.60     Nov 30, 2017

ISS

Z210

European Norm

11.040.01     03.100.70  

Serbian  

Plan 2017.

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Published

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Scope

ISO 13485:2016 specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements. Such organizations can be involved in one or more stages of the life-cycle, including design and development, production, storage and distribution, installation, or servicing of a medical device and design and development or provision of associated activities (e.g. technical support). ISO 13485:2016 can also be used by suppliers or external parties that provide product, including quality management system-related services to such organizations.
Requirements of ISO 13485:2016 are applicable to organizations regardless of their size and regardless of their type except where explicitly stated. Wherever requirements are specified as applying to medical devices, the requirements apply equally to associated services as supplied by the organization.
The processes required by ISO 13485:2016 that are applicable to the organization, but are not performed by the organization, are the responsibility of the organization and are accounted for in the organization's quality management system by monitoring, maintaining, and controlling the processes.
If applicable regulatory requirements permit exclusions of design and development controls, this can be used as a justification for their exclusion from the quality management system. These regulatory requirements can provide alternative approaches that are to be addressed in the quality management system. It is the responsibility of the organization to ensure that claims of conformity to ISO 13485:2016 reflect any exclusion of design and development controls.
If any requirement in Clauses 6, 7 or 8 of ISO 13485:2016 is not applicable due to the activities undertaken by the organization or the nature of the medical device for which the quality management system is applied, the organization does not need to include such a requirement in its quality management system. For any clause that is determined to be not applicable, the organization records the justification as described in 4.2.2.

Related directives

Directives related to this standard.

90/385/EEC

Active implantable medical devices

Harmonized
93/42/EEC

Medical devices

Harmonized
98/79/EC

In vitro diagnostic medical devices

Harmonized
2017/745

Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC

Harmonized
2017/746

Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 on in vitro diagnostic medical devices and repealing Directive 98/79/EC and Commission Decision 2010/227/EU

Harmonized

Life cycle

PREVIOUSLY

WITHDRAWN
SRPS EN ISO 13485:2014

NOW

PUBLISHED
SRPS EN ISO 13485:2017
60.60 Standard published
Nov 30, 2017

Related project

Adopted from EN ISO 13485:2016/AC:2016

Adopted from EN ISO 13485:2016

Adopted from ISO 13485:2016

Regulation

"Сл. гласник РС" бр. 84/2018 Sl. glasnik RS, br. 84/2018
PRAVILNIK o registraciji medicinskog sredstva

МИНИСТАРСТВО ЗДРАВЉА

"Сл. гласник РС" бр. 102/2018 Sl. gl. 102/2018
PRAVILNIK o proizvodnji medicinskih sredstava

МИНИСТАРСТВО ЗДРАВЉА