Xtalks Webinars

Xtalks — The Life Science Community™ brings together professionals across pharma, biotech, medtech, healthcare and research. Join our community today.

[Xtalks Webinars @Xtalks]

Hormones influence nearly every aspect of human health. Helen Gregson from the European Society of Endocrinology shares how the organization is advancing endocrine science through policy advocacy, research prioritization and global awareness efforts such as World Hormone Day.

Read more: https://t.co/LdMuSuZLmv

#Endocrinology #HealthPolicy #BecauseHormonesMatter

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As competition intensifies across cardiometabolic disease drug development, how can biotech companies stand out? MetaVia CEO Hyung Heon Kim shares his advice for leaders navigating innovation, clinical development and strategic growth. Listen now at https://t.co/wa5J6tDfte 🎙️

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Master MRD execution challenges in oncology development with (Moderator) Wael Harb, MD, MBA, Patrick Melvin, Jacquelyn Ritchie, MPH and Muaiad Kittaneh, MD, MBA, FACP in this webinar hosted by Syneos.

As MRD becomes a more decisive input in oncology development, execution quality is what determines whether biomarker data are actionable or simply observational. This session explores how protocol design, site readiness, sample workflows, laboratory alignment, and cross-functional governance can strengthen data integrity, reduce operational risk, and improve downstream clinical, regulatory, and commercial value.

Register for this webinar to learn how to turn MRD strategy into executable trial design and align teams early to improve data quality, regulatory positioning, and commercial impact: https://t.co/4wu0fycBxr

#SyneosHealth #OncologyTrials #MinimalResidualDisease #MRD #Biomarkers #ClinicalTrials #OncologyDevelopment #HematologicMalignancies #SolidTumors #ClinicalOperations #RegulatoryStrategy #MarketAccess #Biopharma #LifeSciences

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Accelerate post-FACS workflow decisions with Alain Agnememel, PhD in this webinar hosted by Rockland.

In antibody discovery, sorting is only the beginning, the real bottleneck often comes after FACS when teams must choose between culture-based recovery and direct recombinant expression. The right post-sort strategy can shorten timelines, improve sequence recovery, and help discovery programs balance throughput, selectivity, and resource efficiency.

Register for this webinar to learn how to select the right post-FACS single B cell workflow, compare culture-based and direct expression strategies, and improve discovery speed and hit quality.

Broadcast 1: https://t.co/GpX4RCSbvk
Broadcast 2: https://t.co/xqTbLIjpuE

#Rockland #AntibodyDiscovery #SingleBCell #FACSSorting #BCellWorkflow #Biopharma #LifeSciences #TranslationalResearch #AntibodyEngineering #RecombinantAntibodies #DrugDiscovery #PlatformDevelopment #Biotech #Immunology

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Transform fragmented endpoint oversight with Todd Rudo, MD, Stacey Rumerman, PsyD, Alain Gay, MD and Kevin McCarthy, RPFT, ATSF, FAARC in this webinar hosted by Clario.

As clinical trials generate more complex digital endpoint data, traditional monitoring models can miss critical signals while adding operational burden. This session explores how centralized review, advanced analytics, and expert-led assessment can strengthen patient safety, improve data integrity, and reduce variability across ECG, spirometry, and eCOA endpoints.

Register for this webinar to learn how to reduce trial risk with intelligent endpoint review, strengthen endpoint integrity, and apply AI-supported monitoring strategies in practice: https://t.co/4ZbaZ2Fmar

#Clario #RiskBasedMonitoring #ClinicalTrials #DigitalEndpoints #eCOA #ECGMonitoring #Spirometry #ClinicalDataAnalytics #PatientSafety #DataIntegrity #CentralizedMonitoring #Biopharma #LifeSciences #TrialOversight

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Accelerate faster proof-of-concept in complex oncology development with Luke Gill and Dr. Yong Wang in this webinar hosted by Emerald Clinical.

Rising costs, longer timelines and low success rates are forcing oncology programs to move beyond conventional trial models. Explore how Bayesian designs, master protocols and real-world evidence can improve dose selection, streamline global execution and support earlier, more confident development decisions.

Register for this webinar to learn how adaptive trial strategies can speed safer early decisions, strengthen evidence generation and improve development efficiency: https://t.co/2yZADnMZf3

#EmeraldClinical #OncologyTrials #ClinicalTrials #ProofOfConcept #BayesianDesign #MasterProtocols #RealWorldEvidence #Biopharma #DrugDevelopment #ClinicalOperations #Biometrics #TranslationalMedicine #PrecisionOncology #GlobalTrials

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Transform fragmented clinical trial workflows with Catherine Tyner, Jamie Beck and Ella Stewart in this webinar hosted by AG Mednet.

Clinical teams are being asked to do more across increasingly complex studies, while balancing data quality, compliance, speed, and cross-functional coordination. A phased workflow strategy helps reduce manual effort, improve operational visibility, and create the documented foundation needed to scale automation and deploy AI responsibly in regulated environments.

Register for this webinar to learn how to identify the right workflow starting point, implement optimization in phases, and build the process foundation for responsible AI adoption: https://t.co/FaTUJccZUf

#AGMednet #ClinicalTrials #ClinicalOperations #LifeSciences #Biopharma #TrialOptimization #WorkflowAutomation #ArtificialIntelligence #ResponsibleAI #ClinicalResearch #DigitalTransformation #RegulatoryCompliance #StudyExecution

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Accelerate smarter clinical development decisions with Mark Lovern, PhD, Andrew Hegedus, MBA, Alicia Baker McDowell, DRSc, MS, EMBA, Catherine Laing and Lynda Holcroft in this webinar hosted by Fortrea.

Emerging biotech teams face relentless pressure to move from strategy to execution with limited resources, rising investor scrutiny, and increasingly complex regulatory expectations. This panel explores how integrated scientific, regulatory, clinical, statistical, and market access planning can reduce risk, sharpen decision-making, and improve the path to approval.

Register for this webinar to learn how to accelerate timelines, navigate regulatory pathways, and make stronger go or no-go decisions with real-world case study insights: https://t.co/jDZKXXgcdy

#Fortrea #LifeSciences #Biopharma #ClinicalDevelopment #ClinicalTrials #RegulatoryStrategy #DrugDevelopment #BiotechInnovation #MarketAccess #GoNoGoDecisionMaking #EmergingBiotech #TranslationalMedicine #ClinicalOperations #RegulatoryAffairs

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Small cell lung cancer has long been one of oncology’s toughest treatment challenges, but new momentum is building around tumor biology, T-cell engagers, ADCs and precision-driven strategies. Xtalks spoke with Amgen’s I-Fen Chang about what’s reshaping SCLC research. Read more: https://t.co/Kj5rYdI4be

#SCLC #LungCancer #Oncology #CancerResearch #ClinicalTrials

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Sanjay J. Mathew, MD, President of the Anxiety & Depression Association (@ADAA_Anxiety) of America, shares how the organization is shaping its vision for anxiety and depression care through science-driven education, research translation and clinical excellence. Read more: https://t.co/5b7695HR0O

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In an exclusive Xtalks Pharmaville interview, @PolaryxTx’ Dr. Lisa Bollinger and Dr. Minsu Kang discuss how patient burden, global enrollment and regulatory alignment shape lysosomal storage disorder trials. Read more: https://t.co/Q9FTzgzZrY

#RareDisease #LysosomalStorageDisorders #PediatricRareDisease #DrugDevelopment

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Overcome viral vector scale-up bottlenecks with Emigdio Reyes, PhD in this webinar hosted by Fujifilm Biotechnologies.

As gene therapies advance toward commercial reality, manufacturing remains a defining constraint, from scalability and process consistency to cost of goods and regulatory complexity. This session examines how upstream, downstream, and analytical strategies can strengthen robustness, support tech transfer, and enable more reliable global supply.

Register for this webinar to learn how to identify scale-up bottlenecks, improve manufacturing scalability, and apply proven case study insights to reduce risk and support commercial supply: https://t.co/gzjRvkQxi8

#FujifilmBiotechnologies #LifeSciences #Biopharma #GeneTherapy #ViralVectors #AAV #CellAndGeneTherapy #Bioprocessing #Biomanufacturing #ProcessDevelopment #TechTransfer #Commercialization #BiotechInnovation

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Master IVDR complexity for custom LDT assays with Lorella Di Donato, Martin Roberge, PhD and Marie-Laure Delalande in this webinar hosted by Cerba Research.

As IVDR reshapes expectations for laboratories developing custom assays, teams must align design control, validation strategy, and technical documentation without slowing innovation. This session delivers a practical view of how to strengthen assay robustness, reduce regulatory risk, and build a defensible path to CE marking.

Register for this webinar to learn how to optimize custom LDT assay development, validate performance against IVDR expectations, and prepare compliant technical documentation for CE marking: https://t.co/tPQSe8hMBA

#CerbaResearch #IVDR #LDT #LaboratoryDevelopedTests #IVD #DiagnosticDevelopment #MethodValidation #DesignControl #CEMarking #RegulatoryCompliance #LifeSciences #Biopharma #PrecisionMedicine #ClinicalDiagnostics

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Transform site workflow friction into faster, lower-burden trials with Daniela Duffett, Andrés Escallón and Kathy Kohler in this webinar hosted by Suvoda.

Clinical research sites are being asked to manage rising complexity with fragmented tools, tighter timelines, and limited resources. This session explores how a more connected technology strategy can streamline visit management, assessments, travel, and payments to reduce administrative strain and improve trial execution.

Register for this webinar to learn how to identify where sites face the most friction and how a unified approach to IRT, eCOA, and payments can reduce workload and operational risk: https://t.co/ovUvZPtt0J

#Suvoda #ClinicalTrials #ClinicalOperations #SiteExperience #PatientPayments #PatientTravel #ECOA #IRT #TrialEfficiency #LifeSciences #Biopharma #DigitalHealth #ClinicalResearch #TrialTechnology

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In a new interview with Xtalks, Kevin Caldwell, CEO, Co-Founder & President of @OssiumHealth, shared how banked bone marrow could reduce reliance on live-donor timing and support a more scalable path for off-the-shelf cell therapies. Read more: https://t.co/tJSSIB9LVh

#OssiumHealth #BoneMarrowTransplant #CellTherapy #AllogeneicTherapy #TransplantMedicine

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Mazen Noureddin, MD, MHSc, FAASLD of Summit Clinical Research shares how MASH clinical research may move beyond liver biopsy and toward more efficient, patient-centered approaches. Watch the Xtalks Spotlight video and read the full article at https://t.co/PnG9UDtCQz.

#MASH #SteatoticLiverDisease #LiverDisease #ClinicalResearch #ClinicalTrials #Biomarkers #Diagnostics #XtalksSpotlight #SummitClinicalResearch

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In heavily pretreated ovarian cancer, clinical trial design must account for more than endpoints and consider patient burden and site realities. Xtalks spoke with @Genelux_Corp's CEO Tom Zindrick about reducing friction in late-line oncology trials.

Read more: https://t.co/4fD4MhSQuG

#ClinicalTrials #OvarianCancer #Oncology #PatientCentricity #ClinicalResearch

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Transform peptide manufacturing bottlenecks into scalable innovation with Christelle Bobier and Olof Persson in this webinar hosted by PolyPeptide.

As peptide complexity rises and demand profiles shift, conventional manufacturing models are under growing pressure to deliver flexibility, speed and compliance at once. This session explores how modular design and process intensification can help manufacturers scale more intelligently, streamline technology transfer and build more resilient production platforms.

Register for this webinar to learn how modular design can accelerate scale-up, improve asset utilization and simplify technology transfer for peptide manufacturing: https://t.co/YTrgPyDm65

#PolyPeptide #PeptideManufacturing #ModularDesign #ProcessIntensification #SPPS #BiopharmaManufacturing #PharmaceuticalManufacturing #TechTransfer #ScaleUp #LifeSciences #Bioprocessing #AutomationInPharma #SustainableManufacturing #CDMO

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Master aseptic fill-finish yield challenges with Tyler Rush and Xufeng Sun in this webinar hosted by Sharp.

As high-value biologics and small-batch therapies continue to reshape development pipelines, traditional assumptions around acceptable product loss are becoming increasingly costly. This session explores where yield is lost across sterile fill-finish and how smarter equipment choices, process settings, and operating approaches can help preserve product, control waste, and support compliance.

Register for this webinar to learn how to pinpoint where product loss occurs, apply practical strategies to protect yield, and avoid high-risk tactics that can undermine outcomes: https://t.co/N5pGJ0s9lm

#Sharp #LifeSciences #Biopharma #SterileManufacturing #AsepticFillFinish #FillFinish #Biologics #DrugProduct #CDMO #ManufacturingScience #ProcessOptimization #SmallBatchManufacturing #RegulatoryCompliance #PharmaManufacturing

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Which pharma, biotech and life sciences companies are growing fastest across the Americas? From oncology and rare disease to radiopharmaceuticals and women’s health, here are the companies from the FT/Statista 2026 ranking driving revenue growth through approvals, partnerships, commercial launches and pipeline progress. Read more: https://t.co/N6DCGWOAqP

#Pharma #Biotech #AmericasBiotech #AmericasPharma #LifeSciences #DrugDevelopment