Session leader & speaker
Developing, manufacturing and commercializing advanced therapies
Led a special session examining the development and industrialization of autologous and allogeneic products—and the strategic trade-offs between them.
Speaking · Conferences · Professional societies
Selected invited talks, oral presentations, conference contributions and topics across advanced therapies, translational development and the decisions that connect science with strategy.
Featured speaking
Session leader & speaker
Led a special session examining the development and industrialization of autologous and allogeneic products—and the strategic trade-offs between them.
First & presenting author · Oral
Presented a framework for addressing donor variability and benchmarking functional heterogeneity in mesenchymal stromal cell development.
Invited oral presentation
Invited to present the translational development of an autologous tissue-engineered bone graft in Fort Lauderdale, Florida.
Plenary Best Papers · Oral
Presented MesenCure in the plenary Best Papers session and received the meeting’s Best Paper Award.
Selected conference record
Invited talks, presenting-author contributions and co-authored work are identified separately to keep the record precise.
Cytotherapy 27(5 Suppl):S9.
Cytotherapy 27(5 Suppl):S136.
Cytotherapy 26(6 Suppl):S20–S21.
International Journal of Oral and Maxillofacial Surgery 52(Suppl):12–13 (published 2024).
Cytotherapy 25(6 Suppl):S89–S90.
Cytotherapy 25(6 Suppl):S138–S139.
Showcase presentation; no meeting abstract.
Cytotherapy 24(5 Suppl):S31.
Cytotherapy 24(5 Suppl):S24–S25.
Cytotherapy 24(5 Suppl):S46.
Cytotherapy 23(5 Suppl):S21.
Blood 138(Suppl):2172.
Cytotherapy 22(5 Suppl):S20.
Speaking themes
How scientific evidence changes when it must support development, partnerships, financing and executive decisions.
A practical framework connecting mechanism, translation, manufacturing, regulation, clinical design, market potential and value.
The development, manufacturing, access and commercialization trade-offs between patient-specific and donor-derived products.
Why clinical milestones, manufacturing readiness, market assumptions and financing requirements must form one coherent system.
Lessons from moving science across intellectual property, diligence, technology transfer and venture formation.
Donor variability, functional heterogeneity, potency and the evidence frameworks required for reproducible development.
Speaking invitations