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IVD Performance Evaluation

Aurevia helps manufacturers comply with the clinical evidence requirements of the IVD Regulation.

Performance evaluation

Performance evaluation is a requirement in the In vitro Diagnostic Medical Devices Regulation 2017/746 (IVDR).
It refers to an assessment and analysis of data to establish or verify the scientific validity, the analytical and, where applicable, the clinical performance of a device.

Before any in vitro diagnostic medical device can be legally placed on the EU market, a manufacturer must comply with the requirements of the IVD Regulation. Clinical evidence shall support the intended use of the device and be based on a continuous process of performance evaluation.

Performance evaluation shall demonstrate the scientific validity, analytical performance and clinical performance of the device and it shall follow a performance evaluation plan. The clinical evidence derived from the performance evaluation shall provide scientifically valid assurance that the relevant safety and performance requirements of the IVD Regulation are fulfilled.

AUREVIA

How can we help?

Aurevia helps manufacturers comply with the clinical evidence requirements of the IVD Regulation by:

  • making the performance evaluation plan
  • making plans and reports for analytical performance studies
  • demonstrating the scientific validity through a systematic literature review
  • making plans and reports for clinical performance studies
  • making the performance evaluation report
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Explore our services

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Regulatory plans

 Our experienced professionals help medical device manufacturers develop regulatory plans that support their entire product lifecycle.

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Technical documentation

All medical devices must have documentation available to support its compliance to applicable regulations. Aurevia supports you in planning and developing your technical documentation.

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Electrical Safety IEC 60601

IEC 60601-1 is the basic international safety standard for medical electrical devices and systems.

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Biological Safety ISO 10993

The international standard for the biological safety evaluation process and preparing biological evaluation documentation for medical device manufacturers.

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IVDR compliance for in-house developed tests

Laboratories developing IVDs in-house must maintain technical documentation and Quality Management Systems to comply with the IVDR and national law.

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IVD performance evaluation

In vitro diagnostic medical device (IVD) regulations are set in the EU In Vitro Diagnostics Regulation (IVDR).

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Qualification and classification of medical devices

Our team’s versatile experience and the available tools help in bringing clarity to the most challenging cases.

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Medical software

Let our experts help you understand and adhere to medical device software regulations throughout the entire lifecycle.

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Risk management ISO 14971

We can help you setup and implement a risk management system and prepare risk management documentation.

Contact us for more information

Meeri Säily
Meeri Säily
Sales Director

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