Clinical-Grade and Advanced Technologies in Stem Cells and Extracellular Vesicles — From Bench to Bedside
Elbeltagy Therapeutics, in collaboration with HPNE, is proud to present the first intensive scientific-education day dedicated to the real-world translation of stem cell and extracellular vesicle (EV) technologies into clinical and commercial reality.
Core Topics
- Clinical Stem Cell Platforms
- How therapeutic stem cells are collected, expanded, characterized, cryopreserved, and banked.
- Ethical and regulatory requirements, including donor consent, pediatric donors, eligibility criteria, and long-term traceability.
- Quality control and release specifications for a cell product intended for clinical use.
- Latest advances in stem cell applications in preclinical models and near-clinic programs.
- GMP-grade manufacturing of stem cells, including:
- 3D bioreactor expansion
- Microcarrier-based culture systems
- Chemically defined / xeno-free media
- Extracellular Vesicles (EVs)
- Scalable EV production using controlled, closed processes:
- Ultrafiltration
- Tangential flow filtration (TFF)
- Size-exclusion chromatography (SEC)
- EV batch testing and release criteria: identity, purity, sterility, potency.
- Single-EV characterization technologies and EVs from body fluids as diagnostic tools.
- EV formulation and use in:
- Therapeutic applications (immune modulation, wound repair, chronic and acute disease targets)
- Precision delivery and targeted therapy through EV engineering
- Clinical-grade EV development: opportunities and current challenges
- Plant-derived EVs for cosmetic and skin applications (regeneration, anti-scarring, repair)
- Industry perspective: we will host companies specializing in GMP-grade stem cell production, EV isolation, EV characterization, and EV diagnostics to guide participants on how to build translational pipelines.
Why Attend?
See how stem cells and EVs move from lab work to real, regulated products. Learn how cells and EVs are manufactured, tested, qualified for use, and prepared for clinical and cosmetic applications. Understand what “bench to bedside” truly requires in terms of GMP, documentation, and quality. Meet experts from both academia and industry. After the event, you can submit your own technical questions and get guidance from our network.
Who Should Attend?
Researchers in regenerative medicine and molecular biology, clinicians (including dentists and oral surgeons), biobank and QC leads, graduate students and early-career scientists, startup founders in advanced therapeutics, cosmetic/skin innovation teams, and anyone in Egypt or the MENA region aiming to build a regulated stem cell or EV-based product pipeline.
This day represents a strategic collaboration between Elbeltagy Therapeutics and HPNE to establish a serious, quality-driven pathway for stem cell banking and EV-based therapeutics in the region.
Participation / Registration
- Registration is mandatory and must be completed before the announced deadline (Stay tuned).
- The event will be delivered live online, with real-time interaction.
- Participation is free of charge.
- The date will be announced soon. Please follow this page for updates.
For more information:
Phone: +20 102 704 0566
Email: Info@elbeltagytherapeutics.com
Facebook: https://www.facebook.com/elbeltagytherapeutics
X (Twitter): https://x.com/elbeltagyco
LinkedIn: https://www.linkedin.com/in/elbeltagytherapeutics/
Instagram: https://www.instagram.com/elbeltagytherapeutics/
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