E-TECHNOLOGIES
Customer Testimonial – From CRA To Management
Join Brittany Erlandson, Sr. Manager of Clinical Operations at QuidelOrtho, as she shares her journey from CRA to management and the crucial role of Medidata's EDC system in enhancing efficiency.
Unleash The Power Of IQVIA eCOA: A Deep Dive
Edward Bartels, an expert in eCOA solutions, provides an in-depth overview of the market trends, emerging technologies, and how IQVIA eCOA is pioneering advancements in this space.
The New Era Of Evidence Generation In Clinical Trials
Learn how top pharmaceutical companies are using novel innovations to drive greater speed, scale, and access in clinical research than ever before in this webinar hosted by Musaddiq Khan, Vice President of DCT Solutions at Medable.
The Art Of Accelerated Study Closeout: End Of Study Solutions
Watch as experts from eClinical Solutions and Medidata delve into end-of-study process challenges, the transition to electronic distribution and management, the advantages of leveraging a digital platform, and more.
TMF Completeness: Simple Solutions For A Complex Problem
In this session, two of the top technology minds in TMF management will demonstrate and a simple yet innovative way to measure completeness at any point during the trial.
Casebook Amendments In Vault EDC
Making casebook changes is easy in Vault CDMS, even in active studies. Use the simple, point-and-click interface to deploy changes to specific sites and subjects. Any new forms or fields are then flagged for site personnel to populate retrospectively for existing patients...
IQVIA eCOA: Amplifying The Patient's Voice
Dive deep into the capabilities of IQVIA's eCOA with our expert Edward Bartels. He will focus on how to effortlessly create a diary, schedule site/participant assessments, and intuitively manage translations and compliance.
Notifications And Reminders
Configurable alarms appear as banner alerts on subjects’ devices, while email notifications help sites monitor potential non-compliance and respond to newly uploaded symptom severity data.
Eliminating Custom Functions From EDC
Watch this video to see how companies like ALCON are driving faster study builds and higher quality for complex studies with data-driven rules and dynamics.
Combining De-Identified EHR And Claims Data
Learn how EHR+ Data can improve your understanding of the patient's journey in ophthalmology, urology, and neurology clinical trials.
Closing The "Compliance Gap" In TMF Archiving
Discover how organizations are crossing this “compliance gap” with PhlexTMF for Viewing, an easily accessible TMF archive for internal use, audits, and inspections.
Successful Subject Creation With eCOA, eConsent, & IRT Process Flow
Watch this process video to see how IQVIA’s integrated Interactive Response Technology (IRT) and electronic Clinical Outcome Assessment (eCOA) solution combined with unified platform delivery drives study orchestration and optimization.
Harnessing The Potential Of Patient-Level Data In Clinical Trials
Join our panel of industry leaders as they explore innovative methods and best practices for incorporating fully consented patient data in clinical trials.
The IQVIA Investigator Site Portal
Understand why companies are standardizing operations on a purpose-built, proven platform that empowers sites to succeed and provides sponsors with helpful insights.
IQVIA IRT - Putting The Focus On Driving Value For Our Customers
IQVIA IRT senior leader and expert, Dan Pavitt, highlights key IRT initiatives aimed at enhancing customer value in this Clinical Leader Solutions Expo presentation.
Impacting Sustainability Through Vendor Collaboration, Procurement
Guido D’Agostino, Head of Global Procurement at Chiesi, and Stefan Dürr, Senior Director of Product Management and Client Delivery at IQVIA IRT, delve into their achievements in sustainability.
Selecting And Expanding Your EDC System: A Testimonial From Everest Clinical Research
Everest Clinical Research shares what lead them to strengthen their partnership with Medidata, and expand past the use of Medidata's EDC products too other helpful solutions.
Overview Of Central eSource From CRIO
Central eSource transforms the conduct of clinical trials by replacing disparate, site-specific source templates with a unified, sponsor-designed framework.
Crossing The TMF Compliance Gap With Inspection-Ready Access For Closed Studies
Your drug study is closed, you need inspection-ready access to the Trial Master File, but your CRO is ready to get the TMF out of their system and wants to send you a zip folder full of documents. What do you do? In this session, we explore an innovative new way to ensure...
An Honest Assessment Of eCOAs From A Site Perspective
Listen to what sites have to say about the changing nature of COAs in clinical trials, including the usage of eCOA, its benefits, and ways to improve the technology.
Industry-First eTMF AI: PhlexTMF v21
Pre-trained on millions of documents and embedding the cumulative guidance of Phlexglobal’s TMF experts, uncover how teams can ensure clinical documents are “right-first-time” at document upload.
The Medable Platform: Deep Evidence Generation
Discover how Medable's platform technology enabled a top vaccine developer to accelerate study deployment and recruitment timelines.
The Diversity Imperative: EDC And Inclusive Clinical Trials
In this EDC Showcase, experts delve into the crucial role of EDC in fostering diversity within clinical trials. Discover adaptable solutions for a more inclusive and efficient clinical workflow.
Mastering Scientific Communication Plans Within Medical Affairs
Join industry leaders from Anju and 9 Labs for a presentation on the pivotal role of Strategic Communication Plans (SCP) in medical affairs.
Get Your TMF Health Score
Introducing the TMF Health Score – an expert methodology that provides an “early warning system” to commonly overlooked issues that often lead to inspection findings.
At The Crossroads Of Data: eCOA And Sensors Converging For Novel Insights
Leveraging sensors and eCOA addresses increasing clinical trial complexity and ensures a more efficient and effective study design.
BYOD Is Here To Stay
In this webinar, eCOA experts will explore how to implement a BYOD strategy, relevant BYOD regulatory considerations, and where the market is going from here.
Overcoming TMF Management Challenges For Small And Mid-Sized Companies
Maintaining an inspection-ready Trial Master File is becoming increasingly burdensome, even for teams with significant resources. In this webinar our experts walk through a new, full-service TMF management approach implemented by smaller biopharmaceutical companies. By ad...
Innovations In IRT
Review the latest innovative techniques employed by IQVIA IRT, including innovations in the design, delivery, conduct and monitoring of clinical trials.
Customer Testimonial – Chuck Bradley, Clinical Development & Operations Consultant
In this testimonial, a Clinical Development & Operations Consultant highlights the industry-standard Medidata platform and the significant benefits of using a consistent system across sites.