Webcasts

Available On Demand

The use of real-world data in clinical research is on the rise – but what are the logistics of tokenizing and linking RCT data? Parexel and Datavant discuss how to implement tokenization within a clinical trial in an informative webinar. Tune in to learn more!

Data Linking in Clinical Trials

Wednesday, July, 13th, 2022 at 11am EDT | 10am CDT | 8am PDT
It’s no secret that hybrid and decentralized trials (DCT) are here to stay.

Yet despite adoption, questions, myths, & rumors about what it means to “decentralize a trial,” persist. Find out the truth from Medable.

Everything You Need to Know About Hybrid/Decentralized Trials

Now Available On Demand! Learn best practices to optimize your clinical supply chain management to decrease costs, improve productivity, and increase patient retention for a more successful clinical trial.

Optimizing Clinical Supply Chain Management

Thursday, June 9, 2022 at 11am EDT The right technology integrations can simplify sponsor and site effort while improving the ability to make decisions during clinical studies.  Learn how one vendor/sponsor collaboration produced an IRT eCOA integration that improved data quality and usability, drove new efficiencies for sites and sponsors while optimizing study delivery, management and change management.

Case Study:  Building integrations that reduce site and sponsor burden and improve the patient journey

Thursday, May 26, 2022 at 11am EDT

1.	Learn of a new integrated monitoring approach to speed your trials, improve study quality while mitigating risks
2.	Understand how integrated monitoring solutions are using innovative technology and analytics to streamline and automate processes 

  Integrated Monitoring: Applying technology and analytics to drive monitoring efficiencies

Tuesday, May 24th, 2022 at 1pm EDT|10 am PDT|6pm BST|7pm CEST

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? Technologies that track how studies unfold are essential but putting that information to good use requires turning real-time visibility into actionable data.

Is Oversight a Burden or Pivotal to Operational Efficiency?

Tuesday, May 3, 2022 at 11am EDT | 7am PDT | 3pm BST | 4pm CEST

What can the eClinical technology industry learn from consumer-focused technology companies? They can learn effective approaches that help engage, incentivize, and motivate patients in clinical trials, to improve recruitment and decrease attrition. 

Applying a Consumer Approach to eClinical Technology

Tuesday, March 22, 2022 at 11am EST
In this webinar, IQVIA eCOA leaders Anthony Mikulaschek, Melissa Mooney and J.C. Wilson will explore how to implement a bring your own device (BYOD) strategy within your study, relevant BYOD regulatory considerations, and where the market is going from here. Specific points within this webinar include how the pandemic has furthered the adoption of BYOD, the benefits of BYOD, including reduced patient burden, reduced costs, and increased patient compliance, and how to develop a BYOD strategy and considerations to be made during planning and implementation. 

BYOD is Here to Stay: Considerations for implementing a BYOD eCOA strategy

Wednesday, March 9, 2022 at 11am EDT
Are you looking for a digital approach to protocol training? See the cross-trial solution that’s eliminating repetitive trainings and saving precious time during study start-up, all while boosting quality and auditability.  

Elevating the Site-Sponsor Experience: Learning Management SaaS in Clinical Trials

Thursday, 24th February 2022, 11:00 EST** Data plays a central role within drug discovery and as decentralized trials become more prevalent in the industry, the need to process and engage with enterprise level solutions and the integration of technology to map data to standards become a must. 

As a central conduit to this IQVIA Biostatistics will share the importance of how to maximize end to end efficiencies through compliance to standards and together provide an understanding to how data flow is an integral part of transformative biostatistics technologies and processes can accelerate clinical development across an organization through an innovative outsourcing approach.  

Webcasts: Clinical Operations