Sampling procedures used for acceptance testing of in vitro diagnostic medical devices. Statistical aspectsWhat is BS EN 13975 Sampling procedures for acceptance testing of in vitro diagnostic medical devices about? BS EN 13975 is a European standard that discusses the acceptance testing of in vitro diagnostic medical devices. BS EN 13975 outlines the sampling procedure requirements for acceptance testing of finished in vitro diagnostic medical devices, which require EC verification by a notified body to ensure safety in the operation of in vitro

It helps put robust procedures in place to conserve your resources and save money

Identification

With obedience and compliance to BS EN 60976

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it is advisable to give due consideration to the environmental impact from the product during its life cycle

instrument

BS EN 13975 applies for drawing up sampling plans for finished products according to the requirements laid down for manufacturers' product certification and production quality systems

For the application of the system and for the correct allocation of numbers or their identification

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the 6 stages of the financial planning process defined

Separation

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