http://www.datacubed.com/. Experienced in research methodologies and conducting qualitative and quantitative research in a variety of therapy areas including respiratory, cardiology, oncology, immunology rare diseases and emerging therapy areas. Signant unites eCOA, eConsent, Patient Engagement, IRT, Clinical Supplies and Endpoint Quality into the industrys most comprehensive patient-centric suite an evolution built on more than 20 years of proven clinical research technology. Login; Register now; Toggle navigation. Session Reserved for Worldwide Clinical Trials, Data Management: Programming and metrics in medical device studies, Vast experience of over 20 years in Quality, Regulatory, Processes Improvements and leading cross organization projects, VP Quality Assurance, Regulatory Affairs and Clinical at IceCure Medical, since September 2020, leading the company compliance and clinical affairs, Prior to joining IceCure Medical, held a position of Director of Quality, Regulatory and Customer Support at Applied Spectral Imaging (ASI) and Several positions at Carestream Health (formerly Orex Computed Radiography). http://greenphire.com/. To learn more , please visit our website - 7 - 9 November 2022, Amsterdam . http://www.augustresearch.com/. AI-ML, a Hype or Hope. Outsourcing Clinical Trials New England 2022. Local vendor oversight vs global provider oversight how would you manage this differently? Prior to working at Genentech, she graduated from the Johns Hopkins Bloomberg School of Public Health with a Master of Bioethics. https://www.slope.io/. This enables earlier submissions with the potential of coming to market sooner and recovering R&D investments ahead of projections. This Clinical Trials Conference includes a wide range of Keynote presentations, Plenary talks, Symposia, Workshops, Exhibitions, Poster presentations and Career development programs. 11 th International Conference on Clinical Trials is scheduled to be held during November 09-10, 2023 at London, UK. Genentech Chief Diversity Office, Patient Inclusion And Health Equity. NikZ shows promise against other important fungal diseases. I am the CEO at OrPro Therapeutics, a biotechnology company in San Diego, CA developing biologic drug solutions to unmet needs in serious epithelial diseases including cystic fibrosis. Making progress of a complex Interventional device study during covid. His goal is to help you accelerate your clinical research career and be a more effective leader. To learn more , please visit our website - http://www.novotech-cro.com/. To learn more , please visit our website - https://lifesciences.transperfect.com/. For more information please contact Graig Daley Business Development Manager and Jackson Young Business Development Associate atsales@citlabels.com. Find out about the events you can meet the Caidya team at and stay updated about the latest conferences and clinical research events. Subsequently completed a Neurology Residency at Columbia University with additional Fellowship training in Neuro-Oncology at the Mass General Brigham program. To learn more , please visit our website - Why should we collect Sexual Orientation and Gender Identity in Clinical Research Studies? http://www.clindatrix.com/. www.viedoc.com, To learn more , please visit our website - AliveCors enterprise platform allows third-party providers to manage their patients and customers heart conditions simply using state-of-the-art tools that provide easy front-end and back-end integration to AliveCor technologies. Dr. Richard Abelson, President & CEO of Statistics & Data Corporation (SDC), founded the company in November of 2005. Start. CA; X-Mine, CA; Delphian Pharma, CA and Certum LLC, CA). He was Senior Director of Clinical Operations at Pharmacyclics from 2012 to 2017 where he was responsible for the development, implementation and maintenance of the Clinical Operations infrastructure, as well as the GCP inspection hosting platform and processes, and regulatory authority marketing approval inspection hosting. http://www.protrials.com/. To learn more , please visit our website - Presently, Ndidi is the Associate Director, Clinical Quality Assurance & GxP Compliance at Ultragenyx Pharmaceutical Inc. where she has worked for over 6 years. Their experienced research team comprises key opinion leaders, board-certified cardiologists and radiologists, sub-specialty scientists, and highly trained technicians who acquire, evaluate, and report high-quality data through an efficient, cloud-based infrastructure. https://www.chillipharm.com/. Examining the behaviors of clinical trial stakeholders to better understand challenges in patient participation. Who we are; Emmes acquired Casimir in March 2022, and the . To learn more , please visit our website - Anju Software is a customer-first organization providing adaptable life science solutions for clinical research, medical affairs, and data science. Add the event to your calendar. To learn more , please visit our website - ClinDatrix, Inc., a CRO, helps pharmaceutical, biotechnology and medical device innovators with clinical projects ranging from Phase I studies to multinational pivotal Phase III trials and post-marketing studies. Topics: With nearly a decade of home visits learnings, Ellen has a unique perspective on how decentralized clinical trials have changed over the years and what the future looks like. European Union Clinical Trial Regulation: Strategic Considerations, Hyatt Regency San Francisco Airport Hotel Visit our website to learn more about how we deliver a Better Clinical Experience. Minimize site activity- could decentralization and Direct-to-Patient trials be the answer to staff shortages? dpocentre.com. To learn more , please visit our website - Allucent is on a mission to help bring new therapies to light by solving the distinct challenges of small and mid-sized biotech companies. Our mission is to eliminate the barriers to clinical trials by bringing access to people where they live, work and are willing to engage. At Trilogy, medical writing is our passion. Combining medical expertise and deep industry knowledge, we develop bespoke solutions to accelerate your innovative treatment development for patients with unmet needs, one trial at a time. AliveCor, Inc. is transforming cardiological care using deep learning. Before joining Curebase, Wayne served as Vice President at mid-sized Florida based CRO Biorasi, where he helped to lead that company to a successful acquisition by a private equity partner in 2018. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionalscollaborateswith biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Following its virtual success over the COVID lockdowns, we are pleased to forecast the 2022 live edition will attract even more, with a great speaker line up and up to date content. The main program of the conference is discussion and debate on the outsourcing of clinical research. March 14 . During her career she has supported Class 1-3 devices through the entire product lifecycle. Headquartered in Sydney since 1996, Novotech has come to be recognised as the CRO of choice for many US and European biotechnology firms in the Asia Pacific. To learn more , please visit our website - Meghan joined a CNS-focused start up in RTP and has spent the last 15+ years working in the life science technology industry. 12 years at Parexel. Gordon Chu is the Director of Investigations Branch at the Food and Drug Administration (FDA) Division of West Coast Imports (DWCI) within the Office of Enforcement and Import Operations (OEIO). Previously, Bruce held leadership roles at Alkahest, Celerion and Allon Therapeutics, and works closely with the Michael J Fox Foundation, chairing one of their scientific review panels. View Event. From 1990 to 2008 he held various Clinical Operations positions at Abgenix, Pharmacyclics, Quintiles, Covance and Syntex. The DPO Centre has assisted over 600 clients globally, including a broad range of bioscience, genomics, therapeutics, healthcare and pharma companies to comply with EU data protection laws such as the GDPR, the EU Clinical Trials Regulation and specific member state requirements. Exploring new science and a futuristic perspective on AB/AM drug development, Exciting growth of artificial intelligence in medicine, A framework on development of artificial intelligence in medicine, The power of public attention and funding, Business opportunity of artificial intelligence in medicine, What they like to see in an outsourced partner organization, What they would like a partner to know about them / how they work. elluminate softwareanddata driven serviceshave been used by more than 100 life sciencescompanieson over 500 clinical trials to reduce cycle time and improve data quality. https://www.trilogywriting.com/. www.careaccess.com. Pharma/Medical Device/Biotech Delegate - Complimentary Pass Register Now. Explore and learn more about Conference Series : World's leading Event Organizer. www.advanceresearch.com. CROMSOURCE operates offices across Europe and North America. Precision medicine is in our blood, our cells, our genes, and our name. The therapeutic areas include: Cancer, CV, CNS and infectious diseases. Project Leader, Health Equity And Population Sciences, Hoffman La Roche. With 2,000 annual trials and projects, around 200 active clients and global access to source drugs in over 60 countries,Myonex is your complete partner around clinical trials around the globe reliable, trusted and by your side. Alexis Garelli has over 15 years of diverse healthcare information and pharmaceutical software technology experience. Despite the ongoing disruptions from COVID-19, 2021 saw some major results from clinical trials. SDC delivers top-tier clinical trial services to pharmaceutical, biologic and device/diagnostic companies. The groundbreaking WATCH-PD study exemplifies how high-dimensional data sources allowing more precise, objective, and higher frequency patient monitoring enable digital biomarker development. IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions and contract research services to the life sciences industry. From 2008 to 2011, he was Senior Clinical Trial Manager at Seattle Genetics where he was responsible for the oversight of multiple oncology clinical trials, as well as support for the development of the Clinical Operations infrastructure and regulatory authority marketing approval inspection hosting. Arena International are delighted to announce Outsourcing in Clinical Trials Europe will be returning to Barcelona on the 3rd-4th May 2023! In addition, 30% of trial participants drop out of the study, Innovation should strive to maximize the synergy of all three variables: safety, efficacy, and speed. November 28-30, 2016 San Antonio, USA. We innovate through pragmatic, forward-looking change that considers the needs of stakeholders in each clinical research role. Why the current state of trials makes it difficult for patients to participate in research, How and when to incorporate patient insights into your programs, How to create a business case to garner support for investing in solutions, The benefit for the study sponsor, and other stakeholders, for investing in solutions to make it easier to be a participant, Barriers to patient participation with a focus on the barrier that became the impetus of the model, Delving into benefits of Patient Navigators and challenges with consistent comprehensive support for patients, Exploring the Enhanced Patient Support Services, Cover proactive strategies to address performance risk and protocol deviations, How to apply performance data from simulation-based training to manage risk areas, Discuss how to interpret and apply learning results to optimize and de-risk your DCT, Rethinking your site management strategy to minimize overburdening sites, dependant on the phase of your study, Pinpointing how site turnover impacts the sponsor and how to help reduce it whilst keeping patient care front of mind. ACM performs more than 20 million laboratory tests each yearspanning all medical disciplines including pathology, microbiology, molecular diagnostics, toxicology and more. Philips BioTel Research is an industry leader in medical imaging and cardiovascular safety testing for clinical trials. We are known for our superior statistical leadership and data management expertise and proud to have supported thousands of studies across a diverse range of diseases. This experience includes in vivo viral- vectored gene therapies, ex-vivo viral vectored and gene edited treatments for oncology and non-oncology patient communities, and RNA medicine modalities. . Actalent is a leading provider of Clinical and Laboratory services. 5 th Clinical Nutrition Conference. Dr. Apfel is a California licensed physician with 20+ years of clinical experience in anesthesiology, critical care medicine, and emergency medicine. Review and assess the selection criteria sponsors face when selecting Phase I jurisdiction. Outsourcing In Clinical Trials East Coast 2022. Explore online site training as a less time/labour intensive way to educate site. She also had several leadership positions with PharmaNet Development Group (now Syneos Health), ICON Clinical Research and eMetagen Corporation. Review market analysis on location of Phase I studies and discuss why these choices are made. Data-driven operations and oversight with elluminate. She was an assistant professor at Loyola University Chicago and a practicing vascular surgeon in Shanghai, China. 25 people interested. As an international key opinion leader in dermatology clinical development, Dr. Jankicevic has served as advisor to multiple companies on their path to global regulatory and commercial success. www.agilexbiolabs.com. Any Where. There, he employed a broad range of methodologies, including: visual psychophysics, neuropsychological and computer-based cognitive assessments, eye tracking, electrophysiology, and structural imaging.