Webcasts

Adoption of remote and virtual trial tools is helping to ensure the safety of dermatology patients during the pandemic. IQVIA Biotech shares how incorporating patient-centric approaches in future dermatology trials can increase patient access and engagement. Live: Tuesday, Jul. 21, 2020 at 11am EDT On demand available after airing until Jul. 21, 2021. Register free

Did you know that across all trial phases, 53% of trial protocols need to be amended after initiation, disrupting the progress of a trial and leading to costly delays? Join our webcast to learn how to position your trials for success from day one. Live: Wednesday, Jul. 15, 2020 at 11am EDT | 8am PDT| 4pm BST | 5pm CEST On demand available after airing until Jul. 15, 2021. Register free

In this exclusive webcast, cutting-edge researchers from the Department of Hematology & Hematopoietic Cell Transplantation share their most recent experiences reprogramming T cells with chimeric antigen receptors (CARs) to tackle both hematologic and solid tumors. Live: Wednesday, Jun. 24, 2020 at 12pm EDT | 1pm CDT | 9am PDT On demand available after airing until Jun. 24, 2021. Register free

Join Steve Rosenberg, Senior Vice President and General Manager, and Jim Streeter, Global Vice President of Product Strategy from Oracle Health Sciences discuss why a transformative shift in clinical data collection needs to happen now, and how leveraging a unified platform can reduce operational inefficiency and streamline workflow in clinical studies. Learn how to move beyond EDC to collect and effectively use data from any source in Clinical One. Live: Tuesday, Jun. 23, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until Jun. 23, 2021. Register free

Hear from R&D experts, Bazgha Qutab and Sharma Ramanathan, on key trends shaping clinical trials and how clinical ops leaders can not only navigate through disruption, but thrive, in order to bring new therapies to patients faster. Live Q&A to follow. Live: Wednesday, Jun. 17, 2020 at 10am EDT | 9am CDT | 3pm BST | 4pm CEST On demand available after airing until Jun. 17, 2021. Register free

Adoption of remote and virtual trial tools is helping to ensure the safety of cancer patients during the pandemic. IQVIA shares how incorporating patient-centric approaches in future oncology trials can increase patient access and engagement. Live: Tuesday, Jun. 9, 2020 at 11am EDT On demand available after airing until Jun. 9, 2021. Register free

The usage of serology-based COVID-19 antibody testing can help us understand the level and prevalence of COVID-19 in communities. Are these tests the ultimate answer? Live: Tuesday, Jun. 2, 2020 at 11am EDT On demand available after airing until Jun. 2, 2021. Register free

Machine learning technologies can help predict outcomes in clinical trials, leading to faster drug approval times, lower costs, and more funding to develop new treatments. How can machine learning deliver business intelligence in the initialization of trials? Live: Tuesday, May 26, 2020 at 1pm EDT | 12pm CDT | 10am PDT On demand available after airing until May 26, 2021. Register free

This webcast provides a step by step look at how to implement new world clinical development approaches into your protocols and develop a strategy for capturing high quality efficacy and safety data, while also facilitating compliance and optimal use of technology. Live: Thursday, May 21, 2020 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST On demand available after airing until May 21, 2021. Register free

Clinical trials are being impacted by COVID-19 as investigator sites cannot accept visits from patients, CRAs or even site personnel. IQVIA is working with agencies and sponsors to adapt operational processes and move trials to remote monitoring capabilities in a virtual trial approach. Live: Thursday, May 7, 2020 at 11am EDT On demand available after airing until May 7, 2021. Register free

Learn from industry experts how to eliminate compliance risks associated with the up to 65% of sites that lose, never receive, or acknowledge these CDs/DVDs, along with the site audits where findings arise due to data access. Live: Thursday, May 7, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until May 7, 2021.

Simply handing off multi-million-dollar studies to CROs without carefully crafted plans for communications and reporting operational data as the study unfolds is hardly a wise move, yet what kind of oversight is needed? Live: Tuesday, Apr. 28, 2020 1pm EDT | 12pm CDT | 10am PDT On demand available after airing until Apr. 28, 2021. Register free

Join this webinar to understand how technology and innovative approaches to collecting clinical, patient and operational data are automating digital end-to-end processes and delivering streamlined data flow for your clinical trials. Live: Tuesday, Apr. 21, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until Apr. 21, 2021. Register free

Learn more about global regulatory acceptance of real-world evidence in a regulatory submission. Understand how to identify opportunities to incorporate real-world Evidence in your submission package. Live: Tuesday, Apr. 7, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until Apr. 7, 2021. Register free

Patient-facing digital technologies are playing an increasingly important role in clinical trials, to the point where including virtual components in trials has become mainstream. Join Kathy Vandebelt, Global Head of Clinical Innovation at Oracle Health Sciences to discuss where the industry stands on terms like "virtual" or "decentralized" trials, what are the benefits and challenges, and what does the future hold for all of us involved. Live: Thursday, Mar. 12, 2020 at 11am EDT | 8am PDT | 3pm GMT | 4pm CET On demand available after airing until Mar. 12, 2021. Register free

In this webcast, Safety Experts – Dr. Mirza Rahman from Otsuka and Bruce Palsulich from Oracle Health Sciences - will discuss the current, near, and longer-term opportunities for Artificial Intelligence in Pharmacovigilance. Live: Thursday, Feb. 27, 2020 at 11am EST | 8am PST | 4pm GMT | 5pm CET On demand available after airing until Feb. 27 2021. Register free

Enter a new era of clinical development planning. Use the power of “big data” and machine learning to generate more accurate plans that embrace uncertainty. Learn how to improve your development planning strategy while reducing trial costs and durations. Live: Thursday, Jan. 30, 2020 at 11am EST | 10am PST | 4pm GMT | 5pm CET On demand available after airing until Jan. 30, 2021. Register free

Trying to incorporate data collected from new patient-facing technology into a traditional protocol design and operational practices just won’t work. Join Kathy Vandebelt, Global Head of Clinical Innovation at Oracle Health Sciences to learn ways to optimize data flow in hybrid and decentralized trials to improve patient experience, data quality, and expedite the clinical trial process. Live: Tuesday, Jan. 28, 2020 at 11am EST | 8am PST | 4pm GMT | 5pm CET On demand available after airing until Jan. 28 2021. Register free

Learn how the diabetes management space is evolving with new metrics such as time in range (TIR), time below range (TBR) and time above range (TAR) growing prominence and the potential benefits that can be achieved by improvements in these metrics Live: Thursday, Dec. 12, 2019 at 11am EST On demand available after airing until Dec. 12, 2020. Register free

Recent research has emboldened the industry as it moves from traditional to hybrid studies with the promise of greater patient participation and patient access – despite this risk to overall study quality data was cited as the number one concern with decentralized trials. How can these risks be mitigated against? Live: Wednesday, Dec. 11, 2019 at 11am EST | 8am PST | 4pm GMT | 5pm CET On demand available after airing until Dec. 11, 2020. Register free

Regulatory requirements continually change, requiring the use of new innovative approaches, including technology advancement and process automation. Join us and take advantage of lessons learned from your peers to eliminate bottlenecks and leverage up-to-date regulatory intelligence to mitigate risks. Live: Tuesday, Dec. 10, 2019 at 11am EST On demand available after airing until Dec. 10, 2020. Register free

This webcast will look at the scale of AMR, how CROs can assist in the development plan of new antimicrobials and where commercial development of new vaccines may be most effective. It will also provide insights and expert opinion on the potential success of antibacterial vaccination in controlling the rise of AMR and reducing the economic burden of infectious diseases. Live: North America: Thursday, Nov. 21, 2019 at 11am EST | 10am CST | 8am PST On demand available after airing until Nov. 21, 2020. Register free

This webcast will look at the scale of AMR, how CROs can assist in the development plan of new antimicrobials and where commercial development of new vaccines may be most effective. It will also provide insights and expert opinion on the potential success of antibacterial vaccination in controlling the rise of AMR and reducing the economic burden of infectious diseases. Live: Europe: Thursday, Nov. 14, 2019 at 3pm GMT | 4pm CET North America: Thursday, Nov. 21, 2019 at 11am EST | 10am CST | 8am PST On demand available after airing until Nov. 21, 2020. Register free

This complimentary webinar explores top trends influencing oncology clinical development. We will share insights and best practices to help ensure your future oncology trials are designed to be quick and efficient and yield high quality data for the best chance for success. Live: Tuesday, November 12, 2019 at 10am EST On demand available after airing until Nov. 12, 2020. Register free

This webinar will provide an overview of the Japanese regulations and development in the Japanese market. Live: Thursday, Oct. 31, 2019 at 11am EDT On demand available after airing until Oct. 31, 2020 Register free

Recent research has emboldened the industry as it moves from traditional to hybrid studies with the promise of greater patient participation and patient access – despite this risk to overall study quality data was cited as the number one concern with decentralized trials. How can these risks be mitigated against? Live: Tuesday, Oct. 29, 2019 at 1pm EDT | 12pm CDT | 10am PDT On demand available after airing until Oct. 29, 2020. Register free

By using GrantPlan, the industry’s largest investigator grant database, teams can narrow down their budget inputs by choosing procedures that precisely match the protocol. They can also choose the exact rare disease indication. GrantPlan. Make precise decisions that are based on robust data and advanced analytics. Live: Thursday, Oct. 10, 2019 at 11am EDT On demand available after airing until Oct. 10, 2020. Register free: Register free

Are your study teams and sites frustrated by a complicated payment process and needless delays? Contracting and payment experts Jim DiCesare, IQVIA, and Jennifer Campanese, Incyte, will discuss how to incorporate the upstream functions of budgeting, contracting, and data management to streamline workflows and expedite site payments to achieve 30-day payment terms and improve site satisfaction. Live: Wednesday, Oct. 2, 2019 at 11am EDT On demand available after airing until Oct. 2, 2020. Register free: Register free