The people behind your application
Dr. MarcelAlbrecht
Consultant
In life sciences, many years lie between the first idea and market entry. During that time costs accrue for preclinical work, trials, approval and quality assurance with no revenue against them. Financing those phases purely through equity or investor rounds often dilutes more than necessary. Public funding in this sector is therefore rarely a bonus, but a fixed part of the financing strategy. This page covers which projects typically qualify and how funding can be planned across the development phases.
Four developments drive projects in this sector, similar across Europe.
Regulatory requirements have become development work. Clinical evaluation, validation and documentation shape product design and development decisions from the outset.
Long cycles with heavy capital needs. Years pass between research, testing, approval and market entry without reliable revenue.
Digitalisation of care. Software as a medical device, telemedicine and data-driven diagnostics raise new technical and regulatory questions.
Personalised medicine and biotechnology. Cell and gene therapies and companion diagnostics shift production towards more specific processes.
Preclinical and early clinical development
Work whose outcome is not established at the outset, including the methods for testing efficacy and safety.
Medical device development
Design, verification and validation, insofar as technical questions remain open and not only known solutions are applied.
Software as a medical device and digital health
Algorithms, data platforms and applications whose reliability and regulatory conformity still have to be developed.
Biotechnological processes and manufacturing
Process development, scaling up manufacturing processes and work on reproducibility and yield.
Diagnostics and biomarkers
Development and validation of new diagnostic methods, including the data analysis required for them.
Investment in laboratory and production technology
Equipment required for development or later manufacturing, through instruments other than development funding.
In life sciences and health, applications rarely fail because the subject is not relevant. Risk usually arises from how the development phase is classified, from regulatory requirements and from the structure of the partners.
Clinical evaluation, validation, quality management or documentation do not qualify automatically. What decides it is whether they are part of a genuine development risk, or whether they primarily fulfil a regulatory obligation for a product that is already defined.
Many projects need hospitals, research institutes, laboratories or CROs. These partners have to be technically necessary, contractually properly integrated and correctly allocated in the costs. Unclear roles or poorly delimited contracts quickly lead to queries or reductions.
A project can be too early for one programme and too late for another. Between preclinical work, clinical validation, approval and market launch in particular, the exact phase decides which funding instrument fits and what evidence is expected.
We do not start with the application but with the question of which phase your projects sit in and which parts qualify. Our specialists know the programmes and the evaluation practice in this sector.
STEP 1
Review the projects.
We go through your roadmap and separate the parts that qualify from those that do not.
STEP 2
Match the programmes.
We map the qualifying work to the right instruments at regional, national and European level.
STEP 3
Build the applications.
We write against the actual evaluation criteria rather than the project description.
STEP 4
Protect what is awarded.
We keep documentation audit-ready throughout the funded period.
The people behind your application
Consultant
The people behind your application
Consultant
The people behind your application
Senior Consultant
The people behind your application
Consultant
The people behind your application
Manager
Working with Ignite Group took a great deal of pressure off us. Thanks to […] their expertise, we always felt confident that our funding application was in the best hands.
If you have big ideas but don’t want to invest blindly: Phase 1 is your reality check – with funding instead of your own risk.
Working with Ignite was structured and reliable throughout. The holistic approach was particularly helpful […]. We are very satisfied with the result and are happy to keep working with Ignite.
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