21 May 2026 - Utrecht
Speakers
Saskia Theunisse - de Jager | Director of Marketing and Communications | Oncode Accelerator
Oncode Accelerator
Oncode Accelerator is a public-private program which aims to innovate and accelerate the development of new cancer therapies by placing cancer patients at the core of preclinical therapy development.
We realize this through the power of three innovation platforms: Patient Cohorts, Organoids and Artificial Intelligence.
Over 30 partners leverage the full potential of the Dutch innovation ecosystem by building development pipelines for four of the most common types of cancer therapies: Small Molecules, Biologics, Cell and Gene Therapies, and Therapeutic Vaccines.
Our world-class toolbox of state-of-the-art technologies will result in more effective, personalized cancer therapies. This will bring us closer to our overarching vision: outsmarting cancer, impacting lives.
At Innovation for Health, we will announce the opening of our first call and are actively looking for partners in biotech and pharma that can bring lead candidates into our pre-clinical program.
Thilo Buck | Senior Consultant | Progress, Expert in Life Sciences
Thilo is a CMC specialist with over 10 years of academic and industry experience across pharmaceutical development, manufacturing and quality. He brings extensive hands-on experience translating scientific and process development into robust, compliant CMC strategies and documentation throughout the product lifecycle, from early clinical development to late-stage and commercial readiness.
He has supported biotech companies, CDMOs and GMP manufacturing organizations in aligning development, manufacturing and quality requirements with regulatory expectations. His experience spans CMC analytical and proves development, lifecycle management, process understanding, and implementation of control strategies across a wide range of modalities, including small molecules, biologicals, viral vectors, cell therapies, vaccines and radiopharmaceuticals.
Currently, Thilo supports late-stage development teams in preparation for pivotal clinical studies, focusing on CMC integration, study execution, technical reporting and regulatory readiness. His profile combines scientific depth with strong knowledge of GMP and quality systems, enabling effective collaboration across Regulatory Affairs, Quality Assurance, Manufacturing, QC and interactions with health authorities.
Progress - Experts in Life Sciences
Progress provides project management, interim management and consultancy services in the field of Pharmaceutical and Bioprocess Engineering, Manufacturing, Quality Control, Chemistry Manufacturing and Controls (CMC), Technology Transfer, Regulatory Affairs, Validation, Lean Six Sigma / Operational Excellence and Quality Management (GxP, QA, QP/RP).
Progress-holds a leading position in fast and effective support and has an excellent track record of ensuring customers reaching their goals. Our consultants utilize and share their wide knowledge and broad experience to accelerate your projects. Our services are characterized by a multi-disciplinary approach, flexibility, added value and persistence. Continuously training, motivating, inspiring and challenging our employees is a high priority for us.
We accelerate improvement!
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