Kid AID
About the project

Paediatrics and AI – together for children

Kid AID is a research and development project combining the experience of clinicians from the Medical University of Wrocław with the AI engineering competences of Animativ Health.

Kid AID – badanie pediatryczne
Values

What matters to us

Child safety

The youngest patients are at the centre of every design decision – both in terms of technology and ethics.

Clinical collaboration

We combine the experience of paediatricians, AI engineers, researchers and designers in one team with a common goal.

Trust and compliance

We process data in accordance with GDPR, and the system is designed with MDR regulations in mind.

Mission

Our goal

The aim of the project is to create a multimodal AI system that supports doctors in assessing the general condition of children aged 0–30 months – a group where early clinical assessment is the most difficult and most critical.

  • Objectification of the doctor's clinical observations
  • Training of medical staff in paediatrics
  • Building the largest Polish paediatric database
  • Implementation of a system certified as a medical device
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Year founded
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Clinical centres
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Partner institutions
0-30mies.
Patient age
Research, ethics, safety

Responsible AI in paediatric medicine

Kid AID is designed with full respect for the privacy of children and their families and in accordance with the highest standards of medical research ethics.

Our approach to data

Recordings made in clinical settings, during routine paediatric examinations, in a non-invasive manner
Participation in the project is voluntary
Requires informed consent from the child's legal guardians
Project conducted under the supervision of a bioethics committee
We apply the principle of data minimisation
Bioethics committee: Research conducted within the Kid AID project has received approval from the Bioethics Committee of the Medical University of Wrocław.
GDPR

Privacy protection

Data processing is subject to Regulation (EU) 2016/679 (GDPR) and Polish personal data protection legislation.

Pseudonymisation

Data does not contain information enabling direct identification of the patient.

Encryption

Data stored and transmitted in an encrypted manner.

Access control

Access only for authorised members of the research team.

Minimisation

We collect only the data necessary to achieve the project's objectives.

Right to erasure

Guardians may withdraw consent and request deletion of data at any time.

Security audit

Regular reviews of security measures and data protection procedures.

Regulations

Regulatory framework

EU 2017/745

MDR – Medical devices

The regulatory qualification and classification of Kid AID system components will be conducted in accordance with MDR, taking into account the intended purpose and manner of use of individual modules.

Kid AID Coach
Not a medical device · No MDR certification required
Kid AID Decision Support
Potentially Class IIa · Clinical validation required · Certification in preparation
EU 2024/1689

AI Act – Artificial intelligence

The project is implemented taking into account the requirements of the AI Act. AI systems intended for medical purposes may be subject to requirements concerning risk management, data quality, user information and human oversight.

Kid AID Coach
Low risk (educational purpose)
Kid AID Decision Support
High risk (AI Act) — under assessment · Additional requirements apply

MDR classification influences whether a given AI component qualifies as a high-risk system within the meaning of the AI Act.

Human Oversight

Human oversight

Decision belongs to the doctor

No module of the Kid AID system takes autonomous clinical decisions. AI provides supporting information, but the final decision always belongs to the doctor.

Algorithms are supervised

AI algorithms are validated on clinical data, tested under controlled conditions, subject to continuous performance monitoring and verified by the medical team.

Limitations are communicated

On every product subpage we inform about the system status, functional limitations, areas of uncertainty and conditions for correct use.

AI Governance

Responsible management

Transparency

We communicate openly about what the system does, what it does not do and what development status it is in.

Data quality

Training data comes from real clinical cases, collected in a standardised way across three centres.

Limitations

We openly communicate known limits of the system. Kid AID is not a diagnostic tool.

Continuous oversight

Algorithms undergo regular validation and evaluation, monitored by the medical and scientific team.

Purpose

The system is designed exclusively to support medical staff, not to make autonomous decisions.

For parents and guardians

Frequently asked questions

Will my child be recorded?

Yes, if you give your consent. The recording lasts approximately 60 seconds and is made during a routine examination.

How is my child's data protected?

All data is pseudonymised and encrypted. Access is restricted to authorised members of the research team.

Can I withdraw consent?

Yes, at any time. Your child's data will be deleted from the database.

Who will see the recording?

Recordings are used exclusively for scientific and educational purposes within the Kid AID project.