Bringing together nearly 700 professionals, TFS delivers tailored clinical research services in more than 40 countries. 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. Mr. Chu began his FDA career in 2002 as a Consumer Safety Officer (CSO). Dr. Karl McEvoy has over a decade of industry experience in both the vendor and sponsor sides. She is currently managing a Ph3 program in rare liver disease. Our Precision Matching software mines millions of patient records, including unstructured physician notes, to pin-point eligible study patients in real-time. To learn more , please visit our website - What are global biotech executives asking/concerned about when evaluating Phase I study plans? Reem enjoys working in startups bringing forward long-term vision and strategies. Outsourcing In Clinical Trials East Coast 2022. Mr. Larwood co-invented his first two commercial molecules before age 30. This session examines how scientific rigor can be applied to clinical outcome assessments (COAs) even though they are subjective. Before joining Clinical Ink in 2021, he was an Assistant Professor in the Department of Ophthalmology & Visual Sciences at the University of Nebraska Medical Center. Signant Health provides solutions that simplify every step of the patient journey to make it easier for people to participate in, and for sites and study teams to run, clinical trials. 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. This enables earlier submissions with the potential of coming to market sooner and recovering R&D investments ahead of projections. It was through this privileged relationship with patients facing devastating diagnoses that Meghan witnessed first hand the life-saving and life-enhancing effects of medical and therapeutic intervention thus piquing her interest in the drug development process. San Diego Marriott La Jolla. With presentations and panel discussions on all the hottest industry trends and outsourcing challenges. Medical Writing and Healthcare Communications Conference. Richard holds a Ph.D. in Industrial Engineering with a focus on applied statistics, quality, and reliability engineering from Arizona State University (ASU), a Master of Science in Industrial Engineering focused in Operations Research and Production Systems (ASU) and a Bachelor of Science in Engineering in Industrial Engineering (ASU), and is certified as a Six Sigma Black Belt. 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. http://www.augustresearch.com/. http://www.arensia-em.com/. Meghan started her career as a Masters level psychologist working within a medical care team treating patients with ALS and traumatic brain injury. AWT Healthcare manufacturers clinical trial labels. Zigzag aims to provide straightforward, reliable and flexible Quality Assurance and auditing services on a local or global basis. CLOSING KEYNOTE: FDAs role in maintaining a secure and resilient supply chain. https://www.discoverinternational.com/. Any Device. Partnerships in Clinical Trials Europe 2021. With offices in over 100 cities worldwide, TransPerfect is the ideal partner to ensure that your global launch makes a global impact by driving quality, mitigating compliance risk, and enhancing patient engagement. Subsequently, Arun lead the Gastric-Immuno-Oncology Rare Disease Bispecific-T cell-Engager portfolio at Amgen on various aspects of clinical research operations. To learn more , please visit our website - The groundbreaking WATCH-PD study exemplifies how high-dimensional data sources allowing more precise, objective, and higher frequency patient monitoring enable digital biomarker development. Please email me if you'd like to set up a meeting to discuss your upcoming clinical trials: Learn more atwww.clinone.com. Dr. Yunis is a scientist with multidisciplinary training and experience in the mechanism of diseases. 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. 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. Isabel Brown (she/her) currently works on the Inclusive Research and Health Equity team for Genentech's Research and Early Development, Clinical Operations group. Currently a Medical Director/Patient Safety Physician Digital & Devices at Astrazeneca. ACM is certified by the College of American Pathologists (CAP) and the Substance Abuse and Mental Health Services Administration (SAMHSA). To learn more , please visit our website - www.Clario.com, To learn more , please visit our website - The two day, in person conference, Outsourcing in Clinical Trials will deliver top-quality content from industry experts covering all aspects of operational . pril 28-29, 2016 Dubai, UAE. In 2021, ERT and Bioclinica merged to become Clario creating the broadest endpoint technology platform in the industry and enhancing our scientific expertise. She is definitely not afraid of being the least popular girl in the room in order to support patient safety! Join us in Philadelphia, May 10th-11th, to shape best practice on: Refining patient recruitment strategy. Imaging endpoints are often used to support go/no-go decision-making in early phase trials. Executive Director, Clinical Outsourcing and Alliance Management, BridgeBio Pharma, Inc. VP Digital Transformation Strategy, Medable, Sr. Director, Clinical Operations NGM Bio, Vice President, Drug Development, Alto Neuroscience, VP Clinical Trial Financial Management, Medidata, Product Director, Decentralised Trial Technology at YPrime, Health Technology - Clinical Research, Meta, Director, eCOA Science & Consulting, Clario, Associate Director, Quality Culture Excellence, Ultragenyx Pharmaceutical, Solutions Consultant, eClinical Solutions, Associate Director of Clinical Operations, CymaBay Therapeutics, Associate Director, Global Regulatory Clinical Services, Global Outsourcing Director, Development Operations, Ascendis Pharma, Sr. Clinical Operations Professional, Imago BioSciences, Senior Director Of Clinical Affairs , Materna Medical, RN, MSN, CCRC, CCRA, Senior Manager of Clinical Affairs and Field Operations Ancora Heart, Deputy Program Director, Office of Medical Devices and Radiological Health Operations (OMDRHO), ORA, FDA, Director, Global Clinical Shared Services at Stryker Neurovascular, Vice President Of Clinical Affairs, Endogenex, Director, Clinical Programs, Clinical Affairs, ReCor Medical, Director, Database Management, Nevro Corporation, Director Global Patient Safety- Device And Digital Health, AstraZeneca, Medical Director, Patient Safety Physician Digital & Devices, AstraZeneca, VP Quality Assurance, Regulatory Affairs And Clinical, IceCure Medical, Vice President, Product Management, Anju Software. The Calendar Industry Events and Conferences, including SPECIAL DISCOUNTS Coming ATTRACTIONS The 5th Annual Outsourcing in Clinical Trials East Coast Conference will convene in Philadelphia in May 13-14, 2014. 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. Dr. Arvinder Dhalla has more than twenty years of experience in pharmaceutical R&D, project management, regulatory affairs and clinical development across several therapeutic areas. ICON plc is a world-leading healthcare intelligence and clinical research organisation. With over 15 years experience in the industry, Esther has predominantly worked in clinical trial management and data management roles across Europe, North America and South Africa. Together with our client partners, we are fulfilling our purpose of Advancing medicine, improving lives., To learn more , please visit our website - https://www.nucleusnetwork.com/au/. http://www.yprime.com/, To learn more , please visit our website - We are focused on helping our clients to address their most significant and complex drug discovery and development challenges. www.tranquilclinicalresearch.com. These conferences closely focus on the advancements in clinical research and trials. Earlier as a bench chemist, he was the first to make Iotrolan, a CT X-ray contrast agent, generic for decades, replaced in about 2005 by newer agents. Anca has over 15 years of experience in the biopharmaceutical industry, working both on the CRO and the Sponsor side. Prior to her work at Potrero, she was the VP of Business Development at Theranova and led marketing initiatives for C. R. Bard (now owned by Becton Dickinson), in both Shanghai and the U.S. She has also worked as a Board Fellow at the American Red Cross Bay Area, currently serves as a guest lecturer at the University of California, San Francisco and Berkeley, and spent several years in sales and training at Johnson & Johnson. To enquire about sponsorship opportunities for the conference, please contact: To enquire about speaking opportunities for the conference, please contact: Arena International is a global B2B events company for online casino players. Tickets. TFS demonstrates scientific and medical competence across populations and therapeutics, with industry-leading capabilities in: -Dermatology, Immunology and Inflammatory Diseases, -Internal Medicine including Neurology & Respiratory, -Pediatrics, Rare Diseases and Orphan Drugs, Detailed information about TFS, and its business offerings can be obtained through. A healthy discussion on different disciplines in pre . This holistic self-service platform provides faster data access and intelligent analytics, empowering clinical trial teams to think innovatively. theactigraph.com. DCT was previously done out of necessity but are we seeing it as a new world order? AliveCor, Inc. is transforming cardiological care using deep learning. Formed through the merger of IMS Health and Quintiles, IQVIA has more than 58,000 employees worldwide. www.emmes.com, Emvenio Research is a leading decentralized research organization (DRO) providing scalable and hybrid decentralized trial solutions improving clinical trial access to underserved and high-risk populations. The report gives a detailed insight into current market dynamics and . BDO Releases 2022/2023 CRO Insights Report. Passionate about novel tech-enabled medical devices that advance the understanding and treatment of diseases. Amsterdam RAI. Combined, our clinics offer over 200 beds. The last decade of this time has been solely focused on the investigator grant administration domain driving strategy and leading teams implementing payment technology in both BPO and enablement models. Sun, 24 Apr 2022, 09:00 End. Arena International are delighted to announce Outsourcing in Clinical Trials Europe will be returning to Barcelona on the 3rd-4th May 2023! https://www.intrinsequehealth.com/. Ops components of various FIH studies and global P1-P3 drug development programs and post-marketing studies in Oncology, Hematology-Oncology, Immuno-Oncology, Infectious Diseases, Immunology, Metabolic Diseases, Ophthalmology, and Critical Care conducted in North America, Europe, Africa, Central and South Americas, Asia-Pacific regions including Japan, China, So Korea, and Australia *Lead cross-functional teams and successfully contributed to several INDs, NDAs, FDA, EMEA, TGA, and NMPA regulatory filings and approvals of marketed products within HIV/Virology Therapeutic Area *Mentor, motivate, and develop clinical operations teams and direct reports *Strong, flexible, strategic team leader with extensive change management successes *Track record to develop, problem-solve, and execute creative and innovative process improvements and quality efficiencies within development operations *Motivated and driven to continue contributing to drug development in transformative medicines with a focus on unmet medical needs, CLOSING KEYNOTE: ClinOps team focus: Managing relationships, retention and hiring in the new world. Exploring the need for a dedicated regulatory pathway for antibacterial/antimicrobial drugs. 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. To learn more , please visit our website - Long term solutions: could reducing the site certification process be a realistic solution? Advarra integrated solutions connects life sciences companies, CROs, research sites, investigators, and academia at the intersection of safety, technology, and collaboration. CROMSOURCE is an international contract research organization providing a comprehensive services to the pharmaceutical and biotechnology companies. http://www.celerion.com. . We offer customized solutions to fit the needs of each study, patient and site, making it easier for your patients to stick with it. https://www.chillipharm.com/. Should our biggest concern post-covid be remote working? To learn more , please visit our website - To learn more , please visit our website - In this role, Mr. Chu develops, manages, and evaluates inspectional matters for DWCI covering all FDA import activities associated with air and sea port operations in the States of Hawaii, California, Nevada, Oregon, and Washington. We work With HeartTMevery day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. Previously, Arvinder has worked at CV Therapeutics and Gilead Sciences where she led various projects from early discovery to clinical development. assisTek has been paving the way for integrating technology and data collection in clinical trials for over 25 years. His last company, TheraSim, trained over 1 million physicians worldwide and was sold to WebMD in 2013. The conference will bring together pharmaceutical and biotech experts to connect and explore solutions to current challenges associated with clinical trials. He brings over 25 years of product management, consulting, and engineering experience across verticals such as life sciences, enterprise software, healthcare, government, entertainment and manufacturing. Datacubed Health is a pioneering technology company making better science and healthier communities a reality. Arun received a Bachelors degree in Biological Sciences from University of California-Riverside, a Masters degree in Biomedical Sciences from Wayne State University and completed Doctoral degree coursework from Michigan State University College of Human Medicine. This Clinical Trials Conference includes a wide range of Keynote presentations, Plenary talks, Symposia, Workshops, Exhibitions, Poster presentations and Career development programs. Explore and learn more about Conference Series : World's leading Event Organizer. Partnerships in Clinical Trials Europe editions. Debashish earned a PhD in Computer Science from the State University of New York at Buffalo, specializing in the application of AI techniques in document analysis. Currently, Audrey Funwie works in the Patient Inclusion and Health Equity team of Genentechs Chief Diversity Office. David Hadden is the pioneer of AI-driven Virtual Patient Simulation technology. Agilex Biolabs operate a fully quality-assured, FDA-inspected laboratory (ISO/IEC17025 and OECD GLP). Prior to working in FDA, Mr. Solis worked in the Bioresearch field focusing on Medical Device and Drug Application Products after graduating from the University California of Irvine and the University of La Verne. To learn more , please visit our website - https://www.anjusoftware.com/. www.prevailinfoworks.com. Curebase is also pioneering the Bring Your Own Physician (BYOP) model, allowing patients the comfort to make decisions with support from their trusted physician, To learn more , please visit our website - www.curebase.com. To learn more , please visit our website - http://www.novotech-cro.com/. Orbis Clinical is a leading global life science recruitment partner. To learn more , please visit our website - To learn more , please visit our website - To learn more , please visit our website - Dr Morimoto has over 25 years of industry experience in leading project teams in the development of innovative medicines, providing guidance in the design and execution of preclinical, clinical and regulatory strategies with a therapeutic focus in Parkinsons, Alzheimers and frontotemporal dementias. Medocitys platform is the only solution that provides a fully interactive clinical trial ecosystem enabling early decision making and safety monitoring in real time. Rave RTSM streamlines your operations and provides real-time visibility for your study teams. Dr Frances Rubenstein has worked in clinical data management for more than 20 years in both medical device and pharmaceutical companies. www.medpt.com. How data mining clinical trial costs and benchmarks can lead to operational efficiencies, The impact of macroeconomic factors on clinical trials and how to best combat changes, How to reimagine financial stability and planning for clinical trials, Clinical Trials: Success & attritions. dpocentre.com. ICACB 2023: Applied Clinical Biostatistics Conference, Rio de Janeiro (Feb 16-17, 2023) ICAHIPHIM 2023: Advanced Healthcare Informatics and Public Health Informatics Management Conference, New York (Feb 16-17, 2023) ICCPP 2023: Clinical Psychiatry and Psychology Conference, Barcelona (Feb 16-17, 2023) ICEPNR 2023: Exercises for Pediatric . March. 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. Rho, a contract research organization (CRO) located in Chapel Hill, NC, provides a full range of services across the entire drug development process. Our platform allows site staff to pull data from various sources such as EHR and legacy systems automatically into their eCRFs (Fully agnostic) hence helping significantly reduce the double-data entry efforts (demographics, labs, vitals, adverse events, allergies, medications) and time spent with CRAs during monitoring visits.
