View source for ISO13485 - 7.1 Planning of product realization

'''7.1 Planning of product realization'''

The organization shall plan and develop the processes needed for product realization. Planning of product realization shall be consistent with the requirements of the other processes of the quality management system (see [[ISO13485 - 4.1 General Requirements|4.1 General Requirements]]).

In planning product realization, the organization shall determine the following, as appropriate:
a) quality objectives and requirements for the product;
b) the need to establish processes, documents, and provide resources specific to the product;
c) required verification, validation, monitoring, inspection and test activities specific to the product and the criteria for product acceptance;
d) records needed to provide evidence that the realization processes and resulting product meet requirements (see 4.2.4).

The output of this planning shall be in a form suitable for the organization’s method of operations.
The organization shall establish documented requirements for risk management throughout product
realization. Records arising from risk management shall be maintained (see [[ISO13485 - 4.2.4 Control of records|4.2.4 Control of records]]).

NOTE 1 A document specifying the processes of the quality management system (including the product realization
processes) and the resources to be applied to a specific product, project or contract, can be referred to as a quality plan.
NOTE 2 The organization may also apply the requirements given in 7.3 to the development of product realization
processes.
NOTE 3 See ISO 14971 for guidance related to risk management.
[[Category:quality]]

[[Category:ISO13485]]