Our services

One research centre, the full product path

The Innomedic Research Centre is the professional partner for the development and implementation of health-industry and healthcare innovations.

We support projects from the idea, through research and validation, to clinical evidence and market launch. We connect our research, clinical, laboratory, consulting and market-launch competencies in one integrated professional system.

We work with startups, development teams and industry and scientific partners alike, so that innovative solutions become well-founded, measurable and marketable results.

Research, development and innovation

From the research idea to a validated solution.

Professional support for health-industry research and development projects, from formulating the research question through prototype development and testing to laboratory validation.

Bremotech Kft. applies a quality management system according to MSZ EN ISO 9001:2015. We carry out complex engineering or IT tasks with the involvement of our experienced professional partners.

Research, development and innovation

What we undertake

Research stages

Research question

Precise definition of the research aim and the problem to be investigated, setting the development direction, and formulating measurable, testable questions.

Prototype and testing

We turn the development concept into a working prototype, then test its operation and performance with laboratory and technical examinations.

Quality and traceability

We carry out our research and development projects along structured, documented and traceable processes. Our work is supported by a quality management system according to MSZ EN ISO 9001:2015.

Engineering and IT background

With the involvement of our engineering and IT partners, the hardware, the software and the complete measurement system can be aligned with the development.

Consulting

We give direction to development

The success of a development needs more than a good idea: it also needs good decisions, the right expertise and a well-considered development process.

We help determine which path is worth taking, what professional and organisational competencies will be needed, and which decision points should be clarified already in the early stage of development.

With our experience we connect research, clinical, regulatory and organisational aspects, so that the development plan is not only professionally well founded, but also feasible in practice.

Decision preparation

Consulting levels

Product path

We make the development path transparent: we define the main stages, responsibilities, and decision and handover points.

Organisation

We map what roles, competencies, capacities and external partners are needed to carry out the development.

Regulatory path

We identify the authorisation, documentation and validation steps required, so that regulatory requirements are already clear in the early stage of development.

Decision preparation

We explore the alternatives and risks, define the next steps, and provide a professional basis for development decisions.

Clinical trials and device validation

We provide evidence for development

We support the full process of a trial, from protocol design and authorisation through data collection and monitoring to evaluation. By providing an eCRF data-capture system we also support structured and traceable recording of trial data.

Our aim is that the evidence needed for development is produced on a professionally sound basis, in a regulated environment and in line with the intended use.

Our experience in clinical trials and patient care helps ensure that the trial plan is not only methodologically appropriate, but also feasible in clinical practice.

Trial process

Steps of the trial

Protocol

Starting from the trial question, we shape the protocol: we define the objectives, the inclusion criteria, the endpoints and the methodological steps needed for validation.

Authorisation

We prepare the authorisations and documentation required for the trial, and support the implementation of the authority and ethics authorisation process.

eCRF system

An electronic data-collection system for structured, traceable and verifiable recording of trial data.

Monitoring

We follow the proper conduct of the trial, data quality and compliance with the protocol, and we handle any deviations.

Evaluation

Organisation, analysis and evaluation of the trial data in order to determine the result of validation and to ground the further development steps.

Measurements

From measurement to data, from data to a development decision

Examination of the airflow characteristics, resistance and airway deposition of inhalation devices and medicines, using measurement and computer modelling methods.

Our research centre has internationally recognised expertise in airflow modelling and airway deposition calculation. Our measurement and simulation equipment makes it possible to produce the objective laboratory data needed for development. The results support product development, comparative studies and the preparation of validation.

Measurement focus

Laboratory measurements

Flow and resistance

Examination of the flow characteristics and resistance of inhalation devices, with breathing parameters that can be defined across a wide spectrum.

Lung deposition

Calculation and modelling of airway deposition, to determine in what distribution the inhaled aerosol reaches the different sections of the airways.

Aerosol

Examination of the particle-size distribution of the aerosol emitted by the inhalation device, and of other characteristics relevant to airway deposition.

Professional communication

We make research results visible

We support the presentation of research and development project results at national and international congresses, and their publication in national and international journals.

We help shape the professional message of the results, identify the right forums and publication opportunities, and prepare publication and congress materials.

Professional communication is a natural part of R&D and grant projects: presenting the results can serve not only the closing of the project, but also the building of professional relationships and the foundation of new cooperation.

Professional communication

Channels

Professional platforms

Congress

Support for appearance at national and international congresses: preparation of presentations, posters and professional materials for presenting project results.

Professional journal

Support for the publication of research and development results in professional journals.

Professional material

Preparation of summaries, professional briefings and background materials related to research results, for the professional and research audience.

Medical-Sales-Marketing

From development to market launch

Medical, marketing and sales support, from creating professional medical content and planning communication through to sales activity.

We turn development results into a market application: we help define the necessary medical and marketing tasks, and the sales processes required for launch.

Contact

Market launch

Levels of launch

Medical information

With our medical and professional knowledge we support the creation, review and proper wording of professional content.

Marketing support

We define the marketing framework of the market launch: the messages, target groups and communication channels, aligned with the professional audience.

Sales support

Design and organisation of the sales process, with the involvement of the partner sales capacity needed for market launch.