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Submitted URL: https://cs5.cognition-solutions.com/r/b45b74553fcf52b5af4a1abe4?ct=YTo1OntzOjY6InNvdXJjZSI7YToyOntpOjA7czoxNDoiY2FtcGFpZ24uZXZlbnQiO...
Effective URL: https://discover.pharmaignite.com/genetic-conversations-networking-event-invite
Submission: On April 25 via manual from IN — Scanned from DE
Effective URL: https://discover.pharmaignite.com/genetic-conversations-networking-event-invite
Submission: On April 25 via manual from IN — Scanned from DE
Form analysis 1 forms found in the DOM
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In partnership with GENETIC CONVERSATIONS: Inspiring Confidence & Fostering Partnerships For Therapy Development Wednesday May 8th , 2024 National Aquarium, Baltimore 7.00pm - 9.30pm EDT Reserve your place Join us at the Baltimore Aquarium for an evening of meaningful conversation and an engaging evening reception, as experts explore the potential of genetic insights and partnerships that contribute to positive change in therapy development. * Discover ways to ensure reproducibility, product comparability and assay standardization * Understand benefits and barriers of analytical test for lot release specifications with different technologies * Learn about areas of collaboration that can accelerate go-to market timelines Reserve your place ENJOY THE EVENING WEDNESDAY MAY 8TH, 2024 ARRIVAL & NETWORKING 7-7.30pm PANEL DISCUSSION 7.30-8.30pm RECEPTION & EXHIBITS 8.30-9.30pm Reserve your place JOIN THE EXPERTS ENJOY EXCLUSIVE INSIGHTS FROM OUR EXPERT INDUSTRY SPEAKERS. Chandler Walker Product Manager, Digital PCR Instruments Thermo Fisher Scientific View Bio Lingzhi Zhao, PHD VP and Head of Discovery Biology and Gene Therapy NeuShen View Bio Dwight Baker Chief Innovation Officer Resilience View Bio Kinnari Patel, PharmD, MBA President, Head of R&D and Chief Operating Officer Rocket Pharma View Bio Hari Acharya, PHD Director, Process Development Capsida Biotherapeutics View Bio SHARDHA MILLINGTON Consultant Citeline Moderator View Bio PANEL DISCUSSION GENETIC CONVERSATIONS: INSPIRING CONFIDENCE & FOSTERING PARTNERSHIPS FOR THERAPY DEVELOPMENT Cell and Gene therapies have had an immense impact in the life sciences industry thus far, with continued innovation promising more real-world success in patients with high unmet needs. Genetic analyses are essential in the development of novel life-changing therapies for patients from the discovery phase to commercialization. As the novel therapeutics grow more complex and regulatory compliance increases it is important to optimize the drug development processes and workflows to help accelerate time to market. Data risks and compliance remain critical pain points for biopharma companies, especially smaller organizations that lack the resources and funding to support lengthy clinical trials. Therefore, it is imperative that decision-makers are aware of solutions that streamline and expedite cell and gene therapy development. Discussion points will include: * The current gene therapy landscape and associated compliance challenges * How to streamline genetic analysis workflows to bring therapies to market efficiently * Key regulatory considerations for advanced therapies, including specifics on mRNA and cell and gene therapies (CGTs) * Best practices for incorporating compliant technology into genetic analysis workflows * How to build trust and confidence in data through strategic partnerships Reserve your place GETTING THERE National Aquarium 501 E Pratt St, Baltimore, MD 21202 REGISTER NOW Work Email Address* First Name* Last Name* Company* Job Title* State or Province* -- Please Select --Outside the US or CanadaAlaskaAlabamaArkansasAmerican SamoaArizonaCaliforniaColoradoConnecticutD.C.DelawareFloridaMicronesiaGeorgiaGuamHawaiiIowaIdahoIllinoisIndianaKansasKentuckyLouisianaMassachusettsMarylandMaineMarshall IslandsMichiganMinnesotaMissouriMarianasMississippiMontanaNorth CarolinaNorth DakotaNebraskaNew HampshireNew JerseyNew MexicoNevadaNew YorkOhioOklahomaOregonPennsylvaniaPuerto RicoPalauRhode IslandSouth CarolinaSouth DakotaTennesseeTexasUtahVirginiaVirgin IslandsVermontWashingtonWisconsinWest VirginiaWyomingMilitary AmericasMilitary Europe/ME/CanadaMilitary PacificAlbertaManitobaBritish ColumbiaNew BrunswickNewfoundland and LabradorNova ScotiaNorthwest TerritoriesNunavutOntarioPrince Edward IslandQuebecSaskatchewanYukon Territory City* Zip Code* Business Phone* Country* Please SelectUnited StatesUnited KingdomCanadaIndiaNetherlandsAustraliaSouth AfricaFranceGermanySingaporeSwedenBrazil--------------AfghanistanÅland IslandsAlbaniaAlgeriaAmerican SamoaAndorraAngolaAnguillaAntarcticaAntigua and BarbudaArgentinaArmeniaArubaAustraliaAustriaAzerbaijanBahamasBahrainBangladeshBarbadosBelarusBelgiumBelizeBeninBermudaBhutanBoliviaBonaire, Sint Eustatius and SabaBosnia and HerzegovinaBotswanaBouvet IslandBrazilBrit/Indian Ocean Terr.Brunei DarussalamBulgariaBurkina FasoBurundiCambodiaCameroonCanadaCape VerdeCayman IslandsCentral African RepublicChadChileChinaChristmas IslandCocos (Keeling) IslandsColombiaComorosCongoCongo, The Dem. 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Mariana Isls.NamibiaNauruNepalNetherlandsNetherlands AntillesNew CaledoniaNew ZealandNicaraguaNigerNigeriaNiueNorfolk IslandNorwayOmanPakistanPalauPalestinian Territory, OccupiedPanamaPapua New GuineaParaguayPeruPhilippinesPitcairnPolandPortugalPuerto RicoQatarReunionRomaniaRussian FederationRwandaSaint BarthélemySaint Kitts and NevisSaint LuciaSaint MartinSamoaSan MarinoSao Tome/PrincipeSaudi ArabiaSenegalSerbiaSerbia and MontenegroSeychellesSierra LeoneSingaporeSint Maarten (Dutch part)Slovak RepublicSloveniaSolomon IslandsSomaliaSouth AfricaSouth Georgia and the South Sandwich IslandsSouth SudanSpainSri LankaSt. HelenaSt. Pierre and MiquelonSt. Vincent and GrenadinesSudanSurinameSvalbard/Jan Mayen Isls.SwazilandSwedenSwitzerlandSyriaTaiwanTajikistanTanzaniaThailandTimor-LesteTogoTokelauTongaTrinidad and TobagoTunisiaTurkeyTurkmenistanTurks/Caicos Isls.TuvaluUgandaUkraineUnited Arab EmiratesUnited StatesUS Minor Outlying Is.UruguayUzbekistanVanuatuVatican CityVenezuelaViet NamVirgin Islands (British)Virgin Islands (U.S.)Wallis/Futuna Isls.Western SaharaYemenZambiaZimbabwe Are you currently using any of Thermo Fisher’s genetic analysis platforms and/or services?* - Please Select -YesNo, but we are considering such platforms/servicesDon't know If so, what platforms and/or services does your company use? * - Please Select -N/AQuantStudio Real Time PCR instrumentsAbsoluteQ digital PCR instrumentsOther vendors real time PCRApplied Biosystems Sanger SequencingSequencing service providers Are you interested in demoing any of our technologies or speaking to a technical specialist? * - Please Select -Yes, I would like a demoNo, not right now Do you have any dietary requirements? I have read and agree to the below privacy policies By ticking this box, you agree to receive emails from Citeline, and carefully selected partners Lead Source - PI Partner -DSONFCOGTFIQVIAAPPISLBIO Primary Product Interest* #n/aBiomedtrackerBiomedtracker Event APIC&DC&D Marketing ServicesC+D DataC+D Data Intelligence ServiceC+D Data Management ServiceC+D Marketing ServicesC+D NPAC+D PharmacyCiteline Analytics Data FeeCiteline AwardsCiteline Awards SponsorshipCiteline ConnectCiteline ConsultingCiteline Engage Data TransferCiteline One OffConnectConsultingCustom AnalyticsDatamonitor HealthcareDatamonitor Healthcare Forecast APIDatamonitor Healthcare One OffData PackagesEvaluateGB AwardsGB Awards SponsorshipGenerics BulletinGenerics Bulletin Marketing ServicesHBW Marketing ServicesInsight Marketing ServicesInsight PublicationsIn VivoIn Vivo Marketing ServicesMeddevicetrackerMedtech InsightMedtech Insight Marketing ServicesMMITOTC AwardsOTC Awards SponsorshipPatient Diversity APIPatient Proximity APIPharmaPharma 360Pharma ConsultingPharma Insight Marketing ServicesPharma Lead ScorePharma Marketing Services Lead ScorePharmapremiaPharmaprojectsPharmaprojects APIPharmaprojects One OffPink SheetPink Sheet Marketing ServicesPrimal PicturesPrimal Pictures Lead ScoreReal World DataRose SheetRWD ExtractRxScorecardSagient Analytics Data FeeSagient Research One OffScripScrip AwardsScrip Awards SponsorshipScrip Marketing ServicesSitetroveSitetrove APISitetrove DiversitySkiptaSkipta Marketing ServicesStrategic PublicationsStudy FeasibilityTrial Results SummariesTrial Result SummariesTrialScope AtlasTrialScope DiscloseTrialScope IntelligenceTrial SummariesTrial Transparency WebsiteTrialtroveTrialtrove: TrialtimingTrialtrove APITrialtrove Intelligence I would like Thermo Fisher Scientific Group (including its affiliates) to add me to a list to receive information about events, products, services, and promotions which Thermo Fisher believes may be of interest to me via the following channels: Email and Phone. I can withdraw my consent and unsubscribe at any time by emailing reply@thermofisher.com. I acknowledge Thermo Fisher Scientific (including its affiliates) and Citeline will process my Personal Information. This is subject to Thermo Fisher Scientific Inc.’s privacy policy and Citeline’s privacy policy which includes information about my rights. Copyright ©️ 2024 Pharma Intelligence UK Limited (Citeline), a Norstella company Pharma Intelligence UK Limited is a company registered in Pharma Intelligence UK Limited is a company registered in England and Wales with company number 13787459 whose registered office is 3 More London Riverside, London SE1 2AQ. The Citeline Team US Toll-Free: +1 888 670 8900 US Toll: +1 212-600-3520 UK & Europe : +44 (20) 805 20700 Email: clientservices@citeline.com × SHARDHA MILLINGTON Consultant Citeline Moderator Shardha is a consultant at Citeline (formerly Pharma Intelligence) who specializes in cell and gene therapy, working with Biotech and Pharmaceutical companies conducting competitive research and strategic market analysis. Shardha is also active in thought leadership creation, having published articles for Citeline's In Vivo publication, as well as quarterly reports on the Gene, Cell and RNA landscape published as part of a continuing partnership with the American Society of Gene and Cell Therapy. × CHANDLER WALKER Product Manager, Digital PCR Instruments Thermo Fisher Scientific Customer-oriented problem-solver with 4+ years of experience working in a global service and support organization in both customer-facing and internal roles. Self-motivated and confident presenter and communicator with 8+ years of experience leading and collaborating with cross-functional teams. Effective and detail-oriented leader with 12+ years of experience working in and supporting biosciences laboratories in pharmaceutical, clinical, and academic settings. × LINGZHI ZHAO, PHD VP and Head of Discovery Biology and Gene Therapy NeuShen Lingzhi Zhao is the Vice President of Discovery Biology and Head of Gene Therapy at NeuShen. She brings over 20 years of experience in neuroscience drug discovery ranging from target identification, IND-enabling studies, to IND filing. Before joining NeuShen, Dr. Zhao served as a Senior Director of Gene Therapy at Applied Genetic Technologies Corporation (AGTC), where she led a discovery team to develop adeno-associated virus (AAV)-based gene therapy to treat neurological diseases. Prior to that, she worked as a team/program leader with increasing responsibilities at multiple global biopharma including Abbvie, Merck, and Simcere Pharmaceutical groups (USA) to discover different modalities to tackle neurodegenerative diseases. Among many programs that she initiated or led over the course of her CNS drug hunting journey, seven programs have entered late discovery/development or early clinic stages.Before starting her career in pharma industry, Dr. Zhao held a faculty position of Instructor and later Assistant Professor of research in neuroscience at the Appel Alzheimer’s Disease Research Institute, Weill Cornell Medical College. With the support from NIH and Alzheimer’s Drug Discovery Foundation (ADDF), Dr. Zhao and her team built an AAV gene delivery platform and initiated the gene delivery of APOE2 for Alzheimer’s disease program, which has now been advanced to a Phase I/II clinical trial by their clinical collaborators. Dr. Zhao earned her Ph.D. in Neuropharmacology from Sun Yat-Sen University and received her postdoctoral training in the neuroscience division at Eli Lilly & Company followed by a research fellow training in the Department of Neurology at Massachusetts General Hospital, Harvard Medical School. × DWIGHT BAKER Chief Innovation Officer Resilience Dwight Baker is the Chief Innovation Officer at Resilience, a technology-focused CDMO for biomanufacturing, including Cell and Gene Therapies. At Resilience, Dwight is responsible for leading Advanced R&D and external collaborations toward innovative solutions that increase patient access to novel therapeutics. Dwight brings over 20+ years of disruptive new product development focused on creating End-to-End automated platforms that scale to multiple intended uses with modular architectures. Previously, Dwight was at Illumina, where he led their End-to-End Clinical Genomic Solutions, directing teams focused on applying Next Generation Sequencing (NGS) to improve human health with genomics and informatics. These included TruSight Oncology 500, VeriSeq NIPT, CovidSeq, and TruSight Software Suite. In addition, Dwight has held various leadership positions at Gen-Probe and Hologic, developing molecular diagnostics solutions where he has led or contributed to over 22 IVD-approved products, including CBER and PMA submissions for Class 3 products utilizing the TIGRIS and Panther Platforms. Dwight holds dual BS degrees in Biochemistry and Microbiology from Cal Poly, San Luis Obispo, and an MS in Software Engineering from National University. He also serves on the advisory board at UCSD extension for Applied Bioinformatics. × HARI ACHARYA, PHD Director, Process Development Capsida Biotherapeutics Hari Acharya leads process development at Capsida Biotherapeutics, a pre-clinical start-up located in Thousand Oaks, CA. Capsida is a fully integrated gene therapy company with research, process development, and cGMP manufacturing capabilities. Capsida is developing engineered AAV capsids for CNS indications. Engineered AAV capsids are a promising modality to deliver therapeutic cargos and treat genetic diseases. As Capsida advances programs to the clinic, robust manufacturing processes are needed that meet regulatory requirements. Hari has over 5 years of experience in the gene therapy space and 10+ plus years working with recombinant protein. Prior to joining Capsida, Hari worked in various roles supporting process development, clinical, and commercial manufacturing at Biomarin and Bayer. × KINNARI PATEL, PHARMD, MBA President, Head of R&D and Chief Operating Officer Rocket Pharma Dr. Kinnari Patel is President, Head of R&D and Chief Operating Officer for Rocket Pharma, overseeing the global R&D and Technical Operations leadership team with oversight spanning discovery through late-stage development and manufacturing. This includes regulatory, clinical, global program teams, CMC, quality and the development organization. Dr. Patel’s prior responsibilities at Rocket included IR, IT, HR, finance and corporate compliance. Dr. Patel has more than 20 years of R&D experience in rare diseases and across several therapeutic areas including immuno-oncology, oncology, respiratory, virology, transplantation, cardiology and metabolism. Dr. Patel has played a pivotal role in raising approximately $1 billion in financing, overseeing the transition of Rocket to a publicly traded company and facilitating the acquisition of Renovacor. She has helped grow Rocket from a three to about 300-person company with a diverse and inclusive culture. She maintains a strong focus on nurturing talent, leading the creation of Rocket University and the Gene Therapy Drug Development Certificate Program. Dr. Patel also spearheaded the development of the Rocket manufacturing site headquartered in Cranbury, NJ from its inception to a fully operational facility. In addition to her current role, Dr. Patel serves as the Rocket board observer and member of the Audit & Compensation Committee.