Clinical Quality Management

In today’s video I will briefly answer the following question:

 

“Why and how should quality management principles be applied in your clinical investigation?”

 

Transcript:

The inclusion of guidance with regards to clinical quality management, is one of the main changes to the new version of the ISO14155.

Why? To ensure that the clinical investigation is compliant to the ISO14155, the Clinical Investigation Plan and any other applicable standards and regulatory requirements, quality management principles should be applied to the processes of the clinical investigation.

How? Sponsors apply these principles by implementing and maintaining written clinical quality procedures, documenting its compliance to these procedures, and ensuring that all auditing requirements are met.

The clinical quality procedures can be integrated in the applicable sections of the sponsor’s overall quality system

Outro: Looking for In-Depth ISO14155:2020 training? Have a look at www.academy-riannetooten.nl/courses.

Share This Post

Other articles

Clinical Investigations

What has changed in the new ISO14155:2020 standard?

The ISO14155 provides an important guide on the use of Good Clinical Practice in clinical investigations. In the ISO14155 you’ll find the main requirements to: protect the well-being, safety and rights of human subjects in the clinical investigation; assure the scientific relevance of the investigation and the trustworthiness of its results; define what the sponsor

Video

Harmonization EC approval process

In today’s video, I will briefly answer the following question:   “How is the approval process of Ethics Committees harmonized under the MDR?”      Transcript:   Ethics committees are responsible for evaluating a clinical investigation and determine whether ethical principles are being met. Requirements related to ethics committee composition and function are not specified in the

Scroll to Top