Arena International are delighted to announce Outsourcing in Clinical Trials Europe will be returning to Barcelona on the 3rd-4th May 2023! KPS Life (www.kpslife.com) is a stand-alone, global functional service provider (FSP) that offers a clinical outsourcing solution across all phases of clinical drug development. Clinical Chemistry & Laboratory Medicine Conference. In her spare time, Ndidi enjoys creative writing and interior decorating. To learn more , please visit our website - https://www.worldwide.com. Contact us for more information and for a live demo tailored to your use case and needs. She intentionally injects laughter and authenticity into everything she does, and is an advocate for kindness, diversity and inclusion, as well as issues impacting women and children. Dr. Apfel is an internationally known authority on designing, conducting, and publishing highest quality clinical trials with thousands of patients that have changed medical practice with over 100 peer-reviewed publications. Medidata is leading the digital transformation of life science, with the worlds most used platform for clinical development, commercial, and real-world data. Each nurse is trained, tested, and certified as a Certified Mobile on an annual basis in the principles of clinical trial research, GCP, Nurse Guidelines and IATA. To learn more , please visit our website - Check out who is attending exhibiting speaking schedule & agenda reviews timing entry ticket fees. From 2 to 4 November 2021. The Budget Conundrum. Acceleration of clinical development in the worlds fastest growing region, Biotech Market Performance and the impact on Clinical Trials and Operations. To learn more , please visit our website - Program and Alliance Management professional with 15+ years of product development, project management and operations experience within the biotechnology and biopharmaceutical sectors. https://www.medidata.com/en/clinical-trial-products/clinical-data-management/rtsm/, To learn more , please visit our website - https://www.medidata.com/. His PhD research at UC San Francisco established the foundation for PEGylated drugs widely used today. Keeping them can be an even bigger challenge. How do you arrange with and clean the large amounts of data generated? An Introduction to Simulation-Based Training in Clinical Research: De-Risking your Studies in 3 Steps. With presentations and panel discussions on the top industry trends and outsourcing challenges, and . During her career she has advocated for critical partnerships with vendors supporting integration with internal stakeholders. We will synthesize the scientific practices underpinning good instrument design and COA data collection methods and recommend next steps for addressing data collection challenges. AbbVie reports rise in full-year 2022 net revenues; Teva Pharmaceutical reports 5% fall in Q4 2022 revenue; Merck reports 2% increase in worldwide sales in Q4 2022; Companies. In 2010, he became a Supervisor Consumer Safety Officer (SCSO). Today she serves as the Chief Strategic Officer for Potrero Medical, a Hayward, California-based predictive health company developing the next generation of medical devices with smart sensors and artificial intelligence. pril 28-29, 2016 Dubai, UAE. Pharmapack is the European event focal point for the pharma packaging and drug delivery device industry. In a separate article, Manasi Vaidya discovers that, fuelled by the successful use of mRNA vaccines in Covid-19, RNA therapeutics are expected to make larger strides in 2022.. Based on available data, there are emerging trends . Frontageis a CRO providing integrated, scientifically-driven research, analytical and product development services throughout the drug discovery and development process to enable biopharmaceutical companies to achieve their drug development goals. Fusion eClinical Suite is the most adaptable, unified platform that serves as the Connected Hub for all your Clinical Trial and operational data and reporting. Our goal each day, every day is to make sure our partners have whatever they need when and where they need it to execute a successful clinical trial, while also minimizing delays, unnecessary costs, and surprises. To learn more , please visit our website - Clinical Trial Supply New England . I went into industry for post-doctoral studies at the biotechnology research center at Ciba-Geigy Corp. (Novartis) and have over three decades of academic and industrial research and senior management experience in protein and metabolic engineering, bio-based manufacturing, and drug discovery / development. In partnership with customers, we build solution-driven teams working for a healthier future. Clinical Outcome Assessments (COAs): Applying scientific rigor and good instrument design. May 3 - May 4 @ Barcelona, Spain. www.myonex.com. He has supervised the management of a clinical portal, eTMF, CTMS, RTSM, EDC, Coding and Grants solutions. We innovate through pragmatic, forward-looking change that considers the needs of stakeholders in each clinical research role. www.kardia.com. 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. Our mission is to optimize the Clinical Trial Ecosystem, applying industry experience and the latest technology to streamline, secure, and enhance the interactions between sponsors, sites, CROs, and others involved in administering and operating clinical trials. Despite the ongoing disruptions from COVID-19, 2021 saw some major results from clinical trials. To learn more , please visit our website - To learn more , please visit our website - His goal is to help you accelerate your clinical research career and be a more effective leader. It seamlessly integrates with EMR, lab, genetic mapping and APCD data, as well as EDC, CTMS and iRT systems to support site and patient identification. For more information, visit http://www.saama.com. Were your solution. Bruce earned his doctorate in biochemistry from UCLA and completed a postdoctoral fellowship at the University of California Berkeley. She is currently the Founder and CEO of Strategikon Pharma, developer ofClinical MaestroTM, the industrys only end-to-end cloud-based platform for clinical trial budgeting, sourcing and budget management including strategic alliance/partnership management. With the most trusted review solutions, innovative technologies, experienced consultants, and deep-seated connections across the industry, Advarra optimizes research performance, empowers clinical sites, and ensures compliance. Dr Jankicevic holds Doctor of Medicine degree, Master of Medical Sciences degree, and Board-certification in Dermatology and Venereology from the University of Belgrade, Serbia. Commercial Services. During her career she has supported Class 1-3 devices through the entire product lifecycle. Compare and contrast the FDA, MHRA and TGA regulatory requirements for Phase I clinical entry. 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. Conference . Add the event to your calendar. www.viedoc.com. Alton Sartor completed a combined MD/MBA from Tulane University. Additionally, Funwie collaborates with colleagues to co-create educational resources as a part of the core team of the Advancing Inclusive Research Site Alliance, which focuses on addressing disparities in clinical research. All three clinics are strategically co-located within leading medical, research and biotech precincts offering unique access to ancillary services including bioanalytical laboratories, MRI, lumbar punctures, chest X-rays, ophthalmology assessments and others. Founded and operated as a more customer centric and nimblealternative to traditional CROs, KPS offers a full range of services leveraging the latest clinical technologies. Meghan started her career as a Masters level psychologist working within a medical care team treating patients with ALS and traumatic brain injury. Conversis is built on one goal: To provide you with the highest-quality clinical trials translations. We are focused on helping our clients to address their most significant and complex drug discovery and development challenges. Dr. Hsu is anesthesiologist and pain management physician, but also a serial entrepreneur. Boring clinical trials are better clinical trials. http://www.protrials.com/. Since 2000, Anne has held supervisory and branch director positions. In addition to her deep understanding of the unique dynamics of developing novel treatments for rare and complex diseases, Dr. Raymond also leverages her combination of training and experience leading the Gene Therapy Think Tank at Worldwide Clinical Trials. His current work focuses on deep collaboration with an interdisciplinary team of engineers and scientists to successfully integrate data from multiple assessments and sensors, implement high-dimensional feature engineering, and both evaluate as well as apply scalable machine learning algorithms. Mr. Chu has served as a mentor for the Federal Executive Board in Los Angeles, CA. http://greenphire.com/. He worked in fortune 500 companies (Bristol-Myers Squibb Co, NJ-USA and Amgen, CA-USA), mid-size and startups/CROs (Discovery Partners Intl. Altasciences full-service solutions include preclinical safety testing, clinical pharmacology, bioanalysis, program management, medical writing, biostatistics, data management and more, all of which can be tailored to specific sponsor requirements. Tickets. Francis has lead supplier oversight responsibilities for sponsors, CROs and clinical system vendors. Any Where. In this presentation we will discuss the following: Clinical development has shifted from a scientifically driven journey to a patient-focused one. as a Microbiologist, HQ position within the Division of Import Operations in Rockville, MD, working as an Import Compliance Officer and working in the FDA Los Angeles District Office as a Director of Import Operations Branch. Parexel Recognized by Frost & Sullivan with 2022 Global Customer Value Leadership Award . Learn how elluminate delivers: Empowering excellence in supply through digital quality management systems, In this session our guest speaker will address the challenges with these drugs in development and looking at parallels in a medical device regulatory strategy. ARENSIAs outstanding recruitment performance across numerous disease areas substantially reduces the overall number of sites and countries for any early-phase patient trial. Novotech is an Australia based clinical CRO operating across Asia and South Africa. He is also President of SBS Medical Management, a healthcare economic consulting firm for investment banks and Expert Medical Reviews, including the California Medical Board. She currently serves as Vice President of Clinical Affairs at Endogenex, a medical device company developing innovative solutions for the treatment of Type 2 diabetes. His father was a physician who developed an interest in the disease decades ago when the family moved to Bakersfield, California, a focal area for the disease. She is currently Director of Patient Safety Medical Device for AstraZeneca and supports products across the enterprise. Making the patient stories the centre of your study with a focus on feedback, Important topics to address with patients, Best timing and approach to successfully engage patients. She was an assistant professor at Loyola University Chicago and a practicing vascular surgeon in Shanghai, China. Topics include feasibility & site selection, clinical data & technology, patient engagement & enrollment, risk-based monitoring, and budeting & clinical outsourcing. To learn more , please visit our website - The news service . 1333 Bayshore Highway, Burlingame, Dr. Cunningham has over 15 years experience in clinical leadership position in medical device industry, overseeing a full spectrum of clinical development programs ranging from FIM to pivotal to post-market phases. Catalyst Clinical Research is a new generation Clinical Research Organization, serving the unique needs of small-to-medium sized biopharmaceutical companies. Based outside Philadelphia, Pennsylvania, we pride ourselves on being boutique by design and always customer focused. Our collaborative approach helps maximize efficiency and agility by acting as an experienced member of your team. March 14 . 2022 edition of Outsourcing in Clinical Trials & Clinical Trial Supply East Asia Conference will be held at InterContinental Seoul Coex, Seoul starting on 29th November. There, he employed a broad range of methodologies, including: visual psychophysics, neuropsychological and computer-based cognitive assessments, eye tracking, electrophysiology, and structural imaging. November 13-14, 2023 Dubai, UAE. Meraf Eyassu is a Executive Director of Clinical Operations at Terns Pharmaceuticals. Currently he is the CEO of Certum Bio in San Francisco Bay area and honors the co-appointment as the Member of the Board of Advisors, UC Berkeley Postdoc Entrepreneurs Program (BPEP). Specifically for Clinical Trials and RWE studies, Medocitys modular and flexible architecture ensures swift configuration and deployment in less than 4 weeks, through a fully interoperable and connected SaaS cloud database. To learn more , please visit our website - Promedica International is a privately held, full-service CRO providing clinical trial services for the medical device, biotechnology and pharmaceutical industries. How do we move forward from here? Philips BioTel Research is an industry leader in medical imaging and cardiovascular safety testing for clinical trials. http://www.medable.com/, To learn more , please visit our website - Zigzag aims to provide straightforward, reliable and flexible Quality Assurance and auditing services on a local or global basis. CA; X-Mine, CA; Delphian Pharma, CA and Certum LLC, CA). Proven ability to organize and manage late-stage development cross-functional teams completing projects on time with meticulous attention to detail. December 07-09, 2015 Atlanta, USA. This experience has allowed her to understand the nuances that set rare and pediatric studies apart from routine clinical studies and develop proper strategies for clients to execute their studies in real world settings. From early phase, bioanalytical sciences, late phase, post-approval and real-world evidence,Worldwide Clinical Trialsprovides full-service drug development services for central nervous system, cardiovascular, metabolic, general medicine, oncology and rare disease therapies.