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	  Webinar: Considerations in leveraging the Universal AAV Standard for dPCR to assess AAV genomes quantity and qualityThis webinar will explore the utility of a Universal AAV Standard in assessing the quantity and genomic integrity of AAV vectors. 
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	  HI-POCT 2024IEEE-EMBS International Conference on Health Innovations in Point of Care Technology (IEEE HI-POCT) is the premier conference in the areas of Health innovations in point-of-care technologies. In its eighth year, this IEEE EMB Strategic Conference will emphasize funding opportunities and the promise and pitfalls of the journey from idea to patient. 
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	  The Safe and Effective Practice of AAV Gene TherapyJoin the Clinical In Vivo Gene Therapy (CIGT) team at Children’s Hospital of Philadelphia for an exciting one-day educational symposium, as we provide fundamental knowledge on the safe and effective practice of adeno-associated virus (AAV) gene therapy across medical specialties. 
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	  Meeting 1: Patient and Care Partner Perspectives on Safety Considerations for Approved Gene Therapy Treatments for Rare DiseasesThe FDA Center for Biologics Evaluation and Research (CBER) is hosting a public patient listening meeting and opening a docket to better understand patient and care partner perspectives on safety considerations and long-term follow-up for approved gene therapy treatments for rare diseases. 
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	  2024 Policy SummitThe 2024 Policy Summit will include experts on topics such as global regulatory harmonization, clinical development challenges, the payment policy landscape, CGT investment insights, and more. 
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	  3rd Annual Lipid Nanoparticles Development Summit EuropeThe 3rd Lipid Nanoparticles Development Summit Europe is your premier [...] 
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	  Week in RAREWeek in RARE, presented by Global Genes, features the RARE Health Equity Forum and the RARE Advocacy Summit. 
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	  RESI Boston 2024The Redefining Early Stage Investments (RESI) conference series connects start-ups and early-stage investors and strategic channel partners. RESI maximizes fundraising companies’ efforts to find partners who are a fit for their technology and stage of development. 
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	  7th International Conference on CRISPR TechnologiesCRISPR 2024 is an exclusive conference that unites leaders from industry, government agencies, and academia to discuss the latest advancements in genome editing technologies. The program brings together experts from diverse fields to discuss how to safely and effectively translate these cutting-edge technologies to patients, while remaining mindful of the ethical implications. 
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	  Advancing Gene and Cell Therapies for CancerDuring this conference, experts in the field will share their insights on targeting cancer-specific antigens, highlight rational combinations to further enhance the function of CAR engineered cells, describe ground-breaking efforts to engineer CAR engineered cells directly in vivo, and illuminate the biology and risks of viral vector integration. 
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	  2024 STAT SummitBy gathering real operators from the trenches who have not previously spoken out, not just talking heads, this event covers some of the biggest challenges faced by those who want to move advances out of the lab and into the world. They will discuss everything from drug development and technology invention to dealing with regulators, courting investors, and pricing and selling products. 
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	  Advancing Rare Disease Therapies Through an FDA Rare Disease Innovation HubThe Reagan-Udall Foundation for the FDA, in collaboration with FDA’s Rare Disease Innovation Hub, will host a public meeting on October 16, 2024. 
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	  World Orphan Drug Congress EuropeThe World Orphan Drug Congress is the largest and most established orphan drugs & rare diseases meeting of its kind across the globe. 
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	  6th Annual Gene Therapy Analytical Development & CMC SummitThe 6th Gene Therapy Analytical Development & CMC Summit will unite 250+ analytical development, CMC, QC, and process development experts to showcase innovative analytical and process development methods, assess their readiness, and ultimately guarantee safety, quality, efficacy, and consistency of gene therapies to regulators. 
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	  Breakthroughs in Muscular DystrophyJoin ASGCT and the Muscular Dystrophy Association in downtown Chicago for an unparalleled opportunity to delve into the latest advancements in research on gene and cell therapies for muscular dystrophy. 
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	  FDA Scientific Exchange 2024: Advancing Gene Editing Platforms for Rare DiseasesThis Scientific Exchange with the FDA seeks to make progress on therapeutic development for rare conditions that are scientifically feasible but commercially non-viable. 
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	  Real-World Evidence Webinar Series: Integrating Randomized Controlled Trials for Drug and Biological Products Into Routine Clinical PracticeThe Reagan-Udall Foundation for the FDA, in collaboration with the Food and Drug Administration (FDA), is hosting a public webinar as part of a series of webinars for FDA-issued guidance related to real-world evidence (RWE). This latest session in the webinar series will discuss the draft guidance: Integrating Randomized Controlled Trials for Drug and Biological Products Into Routine Clinical Practice. 
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	  Class Considerations on Immunogenicity for AAV Gene Therapy Products: Assessing Current Practice and New DataThis free, public event will explore key immunology-related topics that have implications across the class of AAV gene therapies, including immune responses, antibody testing, and redosing strategies. 
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	  WCBP SymposiumStay tuned for more details 
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	  The Festival of Genomics & Biodata LondonWith well over 5,000 attendees the Festival is now the [...] 
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	  FDA-NIH Rare Disease Day 2025This year, NCATS and the U.S. Food and Drug Administration [...] 
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	  Empowering Patients 2025This inaugural virtual event March 12 and 13, 2025 (9 [...] 
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	  Advanced Therapies 2025The Advanced Therapies Congress is Europe’s largest commerical cell and [...] 
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	  Rare Disease Summit 2025The Rare Disease Summit connects key stakeholders to drive therapeutic [...] 
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	  8th Gene Therapy Development SummitJoin peers to drive gene therapy innovation across translational, clinical, regulatory, and manufacturing tracks. 
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	  CRISPR MEDiCiNE 2025Meet the global CRISPR Medicine community at the second CRISPR MEDiCiNE conference. 
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	  Around the World: Frontline of AAV Vectors for Gene Therapy Research in JapanExplore cutting-edge advancements in the use of AAV vectors for [...] 
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	  Genomics of Rare Disease 2025The 2025 programme will highlight non-coding variants and the implication [...] 
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	  2nd International Conference on Human Genetics and Genetical DisordersHuman Genetics and Genetical Disorders-2025 extend our immense pleasure and honor [...] 
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	  ISCT 2025International Society of Cell & Gene Therapy 2025 Annual Meeting [...] 
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	  ASGCT 2025Stay tuned for more information on ASGCT's 2025 annual meeting. [...] 
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	  Global Observatory for Genome Editing International SummitThe Global Observatory’s 2025 Summit foregrounds questions about biotechnologies that [...] 
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	  Gene Therapy Potency Assay SummitEngage with analytical leads to discuss shared pain points, new [...] 
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	  NIST WorkshopsAt the Workshops on Measurements and Standards for Advanced Therapy, [...] 
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	  Cell & Gene Therapy Products 2025The Cell and Gene Therapy Products (CGTP) Symposium: Manufacturing, Quality [...] 
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	  The State of CRISPR & Genome Editing 2025In The State of CRISPR and Genome Editing virtual summit, GEN brings [...] 
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	  The Festival of Genomics & BiodataThe Festival is designed principally for scientists and clinicians who are [...] 
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	  Patient-Centered Long-Term Follow-up for Gene TherapiesThis webinar will consider patient-centered approaches in the specific context [...] 
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	  Cell & Gene Therapy Summit 2025We cordially invite you to The Global Cell & Gene [...] 
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	  Genome Engineering: CRISPR FrontiersThe specific goal for this meeting is to foster fruitful [...] 
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	  Cell & Gene Therapy World Conference 2025The Cell & Gene Therapy World Conference 2025 (CGTWC 2025), [...] 
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	  NORD® Rare Diseases and Orphan Products Breakthrough SummitShape the future of rare disease treatments, research and policy [...] 
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	  Molecular Therapy Presents: Advancing AAV Technology"Advancing AAV Technology: From Capsid Design to Scalable Manufacturing" - [...] 
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	  Breakthroughs in Targeted In Vivo Gene EditingJoin ASGCT at the Marriott Marquis San Diego Marina, Nov. [...] 
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	  Empowering Patients 2026: A Cell and Gene Therapies SummitThis free, virtual summit from ASGCT will bring together patients, [...] 
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	  ISCT 2026International Society for Cell & Gene Therapy 2026 Annual Meeting [...] 
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	  ASGCT 2026 Annual MeetingBoston, MA or Virtual https://annualmeeting.asgct.org/ 
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