Investigator-Initiated Study

In Precision Diagnosis, we create smart connected systems, upgrade workflows, and generate insights from integrated diagnostics, leading to a clear care pathway and aiming at predictable outcomes for patients.

We are dedicated to supporting Investigator-Initiated Study. In pursuit of excellence, we partner with physicians and institutions worldwide to discover how we can combine the power of imaging, pathology, genomics and longitudinal data with insights from artificial intelligence to drive the right care in the right sequence at the right time.

Investigator-Initiated Study (IIS) Review Qualifications

We mindfully review all IIS study requests with a detailed assessment by a cross-functional team.

IIS Requests will be assessed according to the following criteria:

Clinical and scientific merit
Realistic sample size, timelines, budget, and statistical plan
Compliance with international regulations and guidance documents relating to the protection of human subjects, national standards, and compliance with medical device regulation
Alignment with Philips’s therapeutic/diagnostic areas or areas of interest and with the business strategy
Research should address new ideas, new fields, explore gaps in existing knowledge. Proposal is unique (unnecessarily duplicative)
Principal Investigator (PI) adequate research experience and Institute’s infrastructure to conduct the clinical research study
Research resulting in valuable information regarding clinical outcomes, health economics or reimbursement possibilities

Questions?

If you still have questions after reviewing the content on this site, please contact us at [email protected].

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