http://www.labconnectllc.com/. Communities. Lee King on LinkedIn: #octwestcoast2023 #clinicalresearch #lifesciences An opportunity at Gilead Sciences sparked her move to the West Coast, and she is now settled in the San Francisco Bay Area. elluminate softwareanddata driven serviceshave been used by more than 100 life sciencescompanieson over 500 clinical trials to reduce cycle time and improve data quality. Five gene therapy trial readouts to watch in the first half of 2023 New Omicron variant could threaten vulnerable people this winter Inclusive drugs: designing clinical trials for the pregnant population Chris deep knowledge of the global early phase drug development industry strengthens the tradition of success of Nucleus Network, our customers and partners in Advancing Medicines, Improving Lives. About Press Copyright Contact us Creators Advertise Developers Terms Privacy Policy & Safety How YouTube works Test new features Press Copyright Contact us Creators . Medidata is leading the digital transformation of life science, with the worlds most used platform for clinical development, commercial, and real-world data. IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions and contract research services to the life sciences industry. Prior to working at Genentech, she graduated from the Johns Hopkins Bloomberg School of Public Health with a Master of Bioethics. Artificial intelligence in medicine & clinical trials. Tactical clinical operations in digital health studies, First-hand learnings, breakthrough device system, a case study. Dr. David Anderson is a Senior Scientist at Clinical Ink, where he focuses on the development of digital biomarkers in decentralized and remotely-monitored clinical research. . Currently, Audrey Funwie works in the Patient Inclusion and Health Equity team of Genentechs Chief Diversity Office. Proven ability to organize and manage late-stage development cross-functional teams completing projects on time with meticulous attention to detail. Debashish has previously managed successful eTMF products at Veeva and Medidata, as well as clinical trial imaging tools at Synarc (now part of Clario). We provide a comprehensive digital solution for Ph 1-4 studies with enterprise-level capability that is configurable to be fit for purpose to support biopharmaceutical companies, CROs and research sites. Her background in Biotechnology and proficiency in Data Management solidified her proven ability to identify data integrity risks, and problem solve the most complaint path to drug submissions and approvals. Outsourcing in Clinical Trials (OCT) Southern California 2022 Wayne resides in Miami, Florida. Choose from over 15 fully integrated modules on a single platform: EDC, DM, RTSM/IWRS, CTMS, Inventory Management, ePRO, eConsent, Patient Portal, AE/SAE Tracking, Safety Database, Central/Local Lab, Imaging Management, eTMF, and 24/7 Project and Clinical Data Reporting. What are global biotech executives asking/concerned about when evaluating Phase I study plans? Our full service offering includes clinical program management, biometrics services and regulatory affairs. Pharmaceutical Development. 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. 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. Ellen Weiss is the Vice President, In-Home Solutions, Decentralized Clinical Trials at PCM Trials. His thesis was on the role of the Androgen Receptor in Hormone Refractory Prostate Cancer. We are now in the position now to share our practical experiences with Decentralized & Hybrid Clinical Trials; The bedrock of a successful trial is a well-designed protocol with reliable measurements of biomedical and health-related outcomes to satisfy regulatory standards. March 14 . Pharma/Medical Device/Biotech Delegate - Complimentary Pass Register Now. 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. Peachtree BioResearch Solutions is an Atlanta-based Clinical Research Organization that provides clinical development support services and innovative resourcing solutions to medical device, pharmaceutical, and biotech companies. EVENT - DIA Global Pharmacovigilance and Risk Management Strategies Conference. Importance of teams meeting face-to-face so that human touch and team cohesion isnt lost, Setting up rules and expectations creating space for communication, Strategies for prioritising work and tracking milestones with remote teams, Assessing the impact on the trial of remote vs in-person working; how to find a happy medium, How to best leverage remote trial management platforms, How to best utilize critical and non-critical data validation plans, What trial management services are best provided by the sponsor vs. CRO, How to best manage SOW/budget throughout the course of the trial. Medical Writing and Healthcare Communications Conference. http://www.medable.com/, To learn more , please visit our website - To learn more , please visit our website - More recently, Arun headed to Santen, with a focus on driving operational excellence in Ophthalmology clinical research as Associate Director Global Clinical Development and Operations, where he oversees Phase 1 4 clinical trial conduct. http://www.datacubed.com/. http://greenphire.com/. ESMO TAT, known as "The Home of Phase I in Oncology", is the leading congress focusing on promising new anticancer targets and agents, with a particular emphasis on those in early phase clinical development. CROMSOURCE is an international contract research organization providing a comprehensive services to the pharmaceutical and biotechnology companies. As the worlds largest RCO (Research Consulting Organization), ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. Saama Technologies is the advanced clinical data and analytics company, unleashing wisdom from data to deliver better actionable business outcomes for the life sciences industry. To learn more , please visit our website - THREADs platform and supporting services are helping customers to shorten study launch timelines, reduce study budgets with Virtual Visits, and bring studies from the clinic to patients homes. Reem holds a PhD in genetics from the Hebrew University of Jerusalem. The conference will bring together pharmaceutical and biotech experts to connect and explore solutions to current challenges associated with clinical trials. Medocitys platform captures valuable real-time clinical insights & real-world data, while engaging patients, sites, and sponsors. Founded in 1976, ACRP is a Washington, DC-based non-profit organization with more than 13,000 members who work in clinical research in more than 70 countries. Start. TransPerfect Life Sciences specializes in supporting the global development and commercialization of drugs, treatments, and devices designed to improve and save lives. As a supervisor, he had the opportunity to manage an Import Field Operation Team, an FDA team in the Centralized Examination Stations (CES), and the Los Angeles International Mail Facility. Data-driven operations and oversight with elluminate. 6 th Clinical & Forensic Pathology Conference. www.kardia.com. She also had several leadership positions with PharmaNet Development Group (now Syneos Health), ICON Clinical Research and eMetagen Corporation. GxPs in Cell Therapy and key considerations for Quality and Project Management. By tapping into patients rich and varied health journeys on Inspire, researchers and health practitioners around the world are advancing treatments and making breakthrough discoveries. Clinical Trials Conferences | Clinical Trials Meetings | Japan | USA Emmes acquired Casimir in March 2022, and the . Visit our website to learn more about how we deliver a Better Clinical Experience. She has led clinical development in dermatology and medical aesthetics for pharma/biotech, CROs, medical device and cosmetic companies including RAPT, Innovaderm, Premier Research, Allergan, Leo Pharma, and Murad. www.pro-ficiency.com, To learn more , please visit our website - The conference is tailor-made to address the concerns of trial sponsors based in Texas who are conducting . As specialists in clinical regulatory documentation, we provide a service that is more than just writing. In the life sciences vertical, we help pharmaceutical and medical device companies with clinical trial management, data management, biometrics, medical affairs, regulatory affairs, and quality and compliance initiatives. Pro-ficiency ensures that everyone in your study is compliant with all training requirements. Advice for the ClinOps team to avoid unnecessary patient visits, how does your protocol affect the site? Rhonda has more than 30 years of experience in FDA, starting as an ORA Investigator in Portland, OR before becoming a manager located in FDA's Minneapolis office. The company delivers high-quality laboratory testing and diagnostic lab services in support of both clinical trials research, toxicology and individual patient care. Explore online site training as a less time/labour intensive way to educate site. By accelerating clinical trials on all levels, our solutions support major pharmaceutical, biotech, and medical device companies, as well as renowned research institutions worldwide. To learn more , please visit our website - This presentation will discuss: With increasing site staff/physician burnout and sites taking on less projects, we are still feeling the ripple effect of this on trials. She has held key national leadership roles including advisor within the Obama/Biden administrations global HIV response team, advisor to United Nations leadership and instructor at the CDC and USAID. www.rad-md.net. He played a pivotal role in the development and commercialization of Veltassa (USA and EU), a treatment for hyperkalemia, Intermezzo for MOTN insomnia, Kerydin for onychomycosis, and Eucrisa for atopic dermatitis. https://lifesciences.transperfect.com/, To learn more , please visit our website - Celerion provides full study services including statistics, data management and biostatistics (including PK/PD analysis), and bioanalytical services. He has worked for CROs as well as small and large biotechnology companies. May 02-03, 2016 Chicago, USA. He is a key member of the leadership team responsible for defining the company's go to market strategy and value proposition across the many segments of the pharmaceuticals and device research industry. He has been actively involved on both sides of the business in managing CDMOs and CROs. Harness the power of video evidence in clinical trials with ChilliPharms compliant platform and suite of video services for filming, de-identifying and reviewing clinical outcome assessments. 7th Decentralized & Hybrid Clinical Trials - Dynamic Global Events Ms. OBrien has been conducting clinical research for more than 35 years and has covered multiple functions during that time. Having worked within all major biopharma markets including USA, Japan, China, EU and Australia has enabled him to become a trusted advisor to many customers and help them achieve their clinical drug development objectives. Why expert partners and staff matter; what metrics dont tell. Outsourcing in Clinical Trials Southeast . Global Clinical Trials Connect 2023 2022 London United Kingdom. CA; X-Mine, CA; Delphian Pharma, CA and Certum LLC, CA). 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. 5 th Global Pharmacovigilance Summit. She has a wealth of knowledge and experience having served more than 24 years in ORA managing staff and operations focused on medical devices, radiological health, and MQSA. Philips BioTel Research is an industry leader in medical imaging and cardiovascular safety testing for clinical trials. For the 13 th Annual event, our flagship European clinical show will provide delegates with practical take-aways and solutions to their most current operational and outsourcing challenges in clinical trials . To learn more , please visit our website - For more information, visitwww.eclinicalsol.com, or contact us atinfo@clinicalsol.com. 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. CISCRP Conferences - Clinical Research Industry Since our establishment in 2004, we have conducted over 700 phase I clinical trials, with 80% of our clients consisting of US based biotech and pharmaceutical companies. 25 people interested. Weve all had to sit through several pitches from vendor companies telling us what they can do for us, but now its time to reverse the conversation! He received M.Sc. 8 th Pharmaceutics and Novel Drug Delivery Systems Conference. Ndidi also leads the X2 Women in Biotech Group speaker series and is one of the founding members of the UltraMosaic Employee Resource Group. We atMyonexadd value to our clients by helping them always be prepared for what is next in their clinical trials. Clinical Outcome Assessments (COAs): Applying scientific rigor and good instrument design. ARENSIA is trusted by Leading Pharmaceutical and Biotechnology organizations worldwide. Clinical Research Conferences in 2023/2024/2025 - World Academy of She also has a special interest in innovations that can improve the quality and efficiency of clinical trial execution. To learn more , please visit our website - CHI's 9th Annual Clinical Trial Innovation Summit, November 10-11, 2020, Boston, MA, is multi-track event on best practices needed to optimize clinical trial innovation, planning and management. CISCRP staff is committed to participating and presentingspeaker, chairperson, moderator, advisor rolesin relevant and engaging educational events within the clinical research industry. Promedica International is a privately held, full-service CRO providing clinical trial services for the medical device, biotechnology and pharmaceutical industries. 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. ClinOne, a leader in virtual clinical trial management, provides a single platform technology experience to accelerate clinical trial enrollment and remote patient care, compliance and retention. Despite the ongoing disruptions from COVID-19, 2021 saw some major results from clinical trials. OCT Europe 2022 | SGS - SGSCorp For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. eClinical & Clinical Data Management Innovation Conference 2022 . FDAs role in maintaining a secure and resilient supply chain. Dan Solisfrom TheFDAwill give the closing keynote. For more information, visit http://www.saama.com. Sun, 24 Apr 2022, 09:00 End. Trial enrollment accounts for 60% of the total time of the trial and for 80% of trial failures. Deep 6 eliminates months of manual data validation, to de-risk and accelerate clinical trials, because clinical trials should be a gatekeeper (accelerator), not a bottleneck to innovation. Outsourcing Clinical Trials New England 2022. UPCOMING EVENT. Developing successful communication pathways in a more remote world. Aug 05 International Conference on Clinical Trials in Endocrinology (ICCTE) - Montreal, Canada. Triomics is a technology company offering an enterprise-grade platform for clinical trial sites to automate data collection practices. 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. 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. These conferences closely focus on the advancements in clinical research and trials. Our customized and scalable solutions improve the quality and execution of clinical trials while mitigating costs and allowing clients to retain strategic control. She is acknowledged for her expertise and passion in Data Integrity and Vendor Oversight, and has been recognized as a thought leader in process optimization and standardization as they relate to Inspection Readiness. http://www.novotech-cro.com/, To learn more , please visit our website - Prior to SDCs inception, Richard served on the Board of Directors of Ora, Inc. (www.oraclinical.com) for over 10 years. 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. Explore Modern RTSM Solutions. Translational Drug Development (TD2) is a world-class oncology drug development organization specializing in the development of new oncology medicines. Dr. Hsu is anesthesiologist and pain management physician, but also a serial entrepreneur. To learn more , please visit our website - Dr. Hayat received his Ph.D. in process engineering from INP-Toulouse, France and Post-Doctoral Fellowship from Ecole Polytechnique de Montreal, Canada. We provide personalized patient logistics management, reimbursement, and convenience services to support clinical trial participants. 2023 will see the return of the Clinical Trial Supply Europe conference to Milan where pharma, large and small, alongside biotechs will have the opportunity to discuss, debate and consider new technologies and processes to streamline supply chain operations. Scout Clinical, part of the Meeting Protocol Family, provides stress-free, confidential and personalized travel, expense and compensation management services to clinical trial participants on a global scale. 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. Over 20 years in clinical research, including patient innovation, feasibility, strategy, patient recruitment, retention, site engagement. ACM Global Laboratories is one of the largest global independent central labs in the industry. To learn more , please visit our website - http://www.pcmtrials.com/. Find out about the events you can meet the Caidya team at and stay updated about the latest conferences and clinical research events. Meghan McKenzie works in Patient Inclusion and Health Equity in Genentechs Chief Diversity Office. To learn more , please visit our website - Clinical Trials Europe - Informa Connect Study sponsors and contract research organizations have used Medrio extensively in clinical trials across a wide array of therapeutic areas, with notable success in oncology, infectious disease, and more. 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. Isabel Brown (she/her) currently works on the Inclusive Research and Health Equity team for Genentech's Research and Early Development, Clinical Operations group. 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.

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