iTestis, led by Ass/Prof Ben Tran in collaboration with WEHI, is revolutionising clinical data collection for GCT patients in Australia. It provides a comprehensive solution to the challenges of data collection and analysis in the treatment of germ cell tumours. By collecting high-quality clinical data and linking it with biological specimens, iTestis describes the current practice patterns of Australian clinicians and engages in retrospective research projects and translational studies. It also serves as a platform for registry-based clinical trials. Powered by BioGrid's secure platform, iTestis is setting new standards in GCT patient care. Read more - https://loom.ly/Wy_eCJA
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Clinical Diagnostics Sales Manager- Passionate about sales : Focused on patient care : Driven by customer needs | Early detection | Simplifying Diagnostics | Rapid Testing | Home testing | Kit building | Quality
Will you be at IBMS CONGRESS? Let me know! It’s not long until IBMS Congress 2023 and I would love to catch up with you! You'll find me on Velsera’s booth, so come and say hi and learn about all our offerings, including smart sample-to-result software that can automate your lab’s workflow. You will find us in the Foyer, next to Hall 1, Stand F1. See how FastFinder AI software can revolutionise the way in which diagnostic labs work & the many benefits of incorporating this unique, customisable software to your workflows. Some of the benefits of FastFinder include: *Reduce errors by removing manual steps. *Improve accuracy and consistency in reporting results though automated data analysis. *Save time and costs, no secondary review of results needed, only look at the ones that matter. Want to learn more? You know where to find me! Stand F1 in the foyer.
Are you looking for a solution that combines flexibility and accuracy to create customized clinical reports, setting your lab apart from the competition? Velsera's Clinical Genomics Workspace (CGW) is the one-stop shop for streamlining data transfer, variant calling, interpretation, and reporting. This platform provides a comprehensive solution for therapeutic development for somatic variants by providing a population-based and pangenome reference for more accurate diagnosis. Additionally, through our extensive network of more than 140 global partner sites and our Knowledgebase, CGW grants you access to continually updated diagnostic and therapeutic information, eliminating the need for in-house variant curators and reducing costs and risks. Visit booth #F1 to talk with our specialist at the IBMS Congress 2023 and see how we can help you. Location: Birmingham, UK Dates: Sept. 25 – 28, 2023. #EraOfVelsera #IBMS2023 #PrecisionMedicine
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Something new is coming to PVRI...Introducing our webinar series, PVRI 2023/24 Digital, launching November 2023. The series follows the success of our 2021/22 series and has been developed by Dr Patricia Thistlethwaite, MD, PhD, University of California San Diego. Upcoming webinars: 🌐 PAH risk calculators – state of the art assessment 🌐 Controversies in CTEPH: pro-con debate 🌐 Clinical trials for PAH: what are we learning? 🌐 Enhancing drug development for paediatric PH: an integrative perspective 🌐 Ion channels: pathogenic role & therapeutic intervention in PAH 🌐 Single cell transcriptional profiling in lung health and PAH Learn more about the scientific programme, book onto upcoming webinars or watch recordings of missed webinars here: https://pvri.link/digital #PulmonaryHypertension
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Recently published on The Lancet Digital Health, this article offers an in-depth focus on Digital Therapeutics' clinical trials and their development into the clinical landscape. The interesting insights are based on a research of more than 400 DTx clinical trials initiated, or expected to be initiated, between 2010 and 2030 including, among the available analyzed data, the trial's duration and the Medical Subject Headings categories (MeSH). As GDMH's mission is to be a global player in the deployment of digital medicine solutions in a constantly challenging medical scenario, this article similarly showcases the challenging opportunities clinicians and researchers have in designing inclusive DTx clinical trials which could provide several options of personalised care to prevent individuals' diseases, managing their therapy's journeys. Click the link below to read the full article 👉 https://lnkd.in/dKxXnM_i . #togethermovefirst #digitalmedicine #medicalpractice #clinicaltrials
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By integrating a clinical-grade Knowledgebase with the Clinical Genomics Workspace (CGW), you can quickly make informed decisions regarding patient treatment. The Velsera Knowledgebase offers current information on clinical trials, medical literature, drug labels, and additional relevant data. Utilizing this information, CGW facilitates the automatic assessment of variant significance, enabling the creation of reports that present the most relevant therapeutic options to the treating clinician. This integration not only saves your team time but also ensures the delivery of high-quality clinical results, ultimately leading to the best possible treatment for your patients. Learn more: https://lnkd.in/guXky8s7 #PrecisionMedicine #NGS #Genomics #EraOfVelsera
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FYI upcoming 2024 call from the European Partnership for Personalised Medicine - EP PerMed - the European Partnership for Personalised Medicine - a co-funded Partnership under Cluster 1 (Health) in Horizon Europe. This call aims to fund research that fosters the identification and/or validation of targets for personalised medicine approaches. Applicants submitting a proposal must combine research on new and advanced targets with companion biomarker research (companion diagnostics). Consortia are required to be transnational, interdisciplinary and trans-sectoral, as well as to clearly outline the personalised medicine perspective in the research proposed. The budget is €45m and there will be a 2 stage application process. As this is a co-funded Partnership, it requires simultaneous participation and national co-funding commitment from relevant national research funding bodies. Ireland’s participation in this call is being facilitated and co-funded by both the Health Research Board (HRB) and Science Foundation Ireland. An info day on this call is scheduled to take place the afternoon of January 15, 2024 (TBC). Expected 2024 call timeline as follows: 👉🏻 2nd January: Publication of the call 👉🏻 12th January: Opening of the pre-proposals submission system 👉🏻 15th January (TBC): call info day 👉🏻 5th March: Deadline for pre-proposal submission 👉🏻 around 20 May: Results of the pre-proposal assessment and invitation to the full-proposal stage 👉🏻 20th June: Deadline for full-proposal submission 👉🏻 Mid/end of August: Rebuttal stage 👉🏻 October: Funding decisions to the applicants 👉🏻End of 2024/early 2025: Expected project start (depending on national funding regulations) Maria Nash PhD | Michael Ryan | Patricia Clarke | Irene Castellano Pellicena | Dr Siobhan Hackett
Pre-Annoucement: "Identification or Validation of Targets for Personalised Medicine Approaches (#PMTargets)" - this will be the topic of EP PerMed's first joint transnational call for research proposals. The applying transnational consortia are asked to combine research on new and advanced PM targets with companion biomarker research. The final call text is expected for early January. The full text of the pre-announcement is available here: https://lnkd.in/eDtyf65h #PersonalisedMedicine #EPPerMedJTC2024
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Catch up on the latest #Transplant Sessions 💬🩸 In this session, leading experts Johannes Schröder-Schetelig, MD, DKMS Group and TU Dresden & Gesine Bug, MD, Goethe-Universität Frankfurt, discuss whether patients with #acutemyeloidleukemia (#AML) should receive treatment before #stemcelltransplantation (#SCT), which was presented and debated at the 2023 #SOHO Annual Meeting The experts further discuss findings from the #ASAPtrial (NCT02461537), criteria used for selecting patients for #SCT, how to approach patients with #primaryrefractoryAML, and the impact of #cytogenetics on patient selection for #SCT 🔬 WATCH NOW 👉 https://lnkd.in/ey8TS8Dy #HemOnc #Leusm #AMLsm
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We are thrilled to announce a groundbreaking partnership between PlexusDx and the Australasian Precision Medicine Academy (APMA). This collaboration aims to accelerate the adoption of pharmacogenomics in the USA, leveraging social media and collaborative lab initiatives to educate and empower clinicians. Pharmacogenomics, the study of how an individual’s genetic makeup influences their response to medications, holds the promise of personalized medicine. Through this partnership, we will combine APMA's comprehensive pharmacogenomics education with PlexusDx's advanced genetic testing capabilities. Our goal is to provide healthcare providers with the tools and insights needed to deliver truly personalized patient care, enhancing treatment outcomes and reducing medication-related harm. Together, we are committed to transforming patient care, reducing healthcare costs, and improving the quality of life for patients through precision-driven healthcare solutions. Read more about this exciting collaboration in our latest press release: https://lnkd.in/g9xj2zk8 #PrecisionHealth #Pharmacogenomics #PlexusDx #APMA #HealthcareInnovation #PersonalizedMedicine #PatientCare
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Check out our latest abstract published during #ASCO24 by Antoine IANNESSI, Head of Medical Affairs and hubert beaumont, Clinical Scientist at Median Technologies. This research emphasizes the importance of considering reader variability and adjudication impacts in clinical trials. Key Highlights: 📑 FDA Recommendations: Exploring inter-reader variability in BICR with double reads. ⚠️Challenge: inter-reader variability persists, especially in RECIST evaluations. 🔬 Methods: Analyzed five phase III lung trials (7 readers, 1017 patients) to examine Discrepancy Rates (DR) and bias. ⚖️ Impact of Adjudication: Investigating how adjudication influences Progression-Free Survival (PFS) estimates. 🔗 Read the abstract below or click here: https://lnkd.in/ekSxMcp3 #ClinicalTrials #OncologyResearch #MedicalImaging #LungCancer
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“Why should you prefer an IVDR-certified NIPT test for your patients?” Listen to this short webinar featuring Jennifer Stobbs from Illumina 👉https://lnkd.in/ew_AxQg5 Register now and figure out more about: Reliable Test Results Extensive Clinical Validation External Review and Assessment Regulated Post-Market Surveillance Locally performed tests #NIPT #NGS #illumina #CEIVDR
Innovative technologies
emea.illumina.com
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Can Understanding HO-1 in BACH1 Knockout Mice Help Treat Sepsis Better? Raghavan Pillai Raju, Medical College of Georgia at Augusta University, USA, will present a short oral contribution during #RedoxMedicine2024 elaborating on this topic. Dr. Raju will discuss the regulation of HO-1 in BACH1 knockout mice following sepsis. He will provide new insights into the regulatory mechanisms of HO-1 in response to sepsis, potentially informing new therapeutic strategies. Join us on June 27-28, 2024 at Fondation Biermans-Lapôtre, Paris, to learn more! 🔗 Selected Short Orals: https://lnkd.in/gypa9uFD. 🌐 More information: https://lnkd.in/dkNzFQZU. #RedoxMedicieSociety #RedoxMedicine2024 #biomarkers #redoxbiology #redox #antioxidants #innovation #oxidativestress #RedoxResearch
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