E-TECHNOLOGIES
Preparing For 2022
2022 will be an important year for drug development. There are many questions around changes that came into play during the pandemic. A panel of experts look back over the year and into the future to help you prepare for the coming year.
Functional Work Streams: Operationally Preparing Your Teams For Successful TMF Inspections
Inspection readiness is all about preparation. Not just having your documents in order, but also your team. In this session, seasoned TMF expert McKenzie Knudson will share a proven approach to getting your team ready for inspections.
Castor eConsent: Site View
Study coordinators aim to enroll participants efficiently through a partnership that leverages direct-to-patient marketing to streamline recruitment.
Accelerate Clinical Insights: From Data Deluge To Decisions In Minutes
Unlock clinical trial insights in minutes, not months. Discover a platform that streamlines data review with AI-powered listings and visualizations to empower faster, smarter decisions.
Selecting Medidata Rave: A Testimonial From Richmond Pharmacology
What made the Medidata's Rave EDC system stand out to Richmond Pharmacology during their vendor selection period?
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.
Seamless And Integrated Onboarding For Trial Participants
Streamline your patient experience with a comprehensive, all-in-one solution that allows you to recruit, screen, and enroll participants remotely from the comfort of their own homes.
Innovations In IRT
Review the latest innovative techniques employed by IQVIA IRT, including innovations in the design, delivery, conduct and monitoring of clinical trials.
Maximize Control And Transparency On The Path To Study Go-Live
Simplify the historically complicated, black-box processes around eCOA solution deployment, content storage and visualization, and global go-live.
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.
Should Sponsors Provide Source Document Templates?
Here, we debate sponsor-provided source document templates, weighing regulatory guidance, compliance risks, and operational impacts for smarter clinical trial documentation decisions.
Do You Know Your TMF Health Score?
For inspection-readiness, the critical attributes of TMF health are completeness, timeliness, and quality. View our experts explore what your TMF Health Score could be and how this can be used to achieve and maintain ongoing TMF health and inspection readiness.
Defining And Implementing The Right Oncology Digital Strategy
A panel of oncology experts shares how top life science companies are using a combination of DHTs, ePROs, clinical trial platforms, and more to ease oncology research and drastically reduce timelines.
What It Really Takes To Adopt eConsent Across Large Pharma
Explore the benefits of incorporating consent management technology and discover practical strategies for developing effective change management and training programs.
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.
Introducing A Smarter, More Cost-Effective Way To Run Clinical Trials
While early-phase trials often rely on less capable, cost-effective systems, the transition to more complex studies in later phases necessitates a more robust EDC system.
eTMF Innovation
Watch the available video to see how AI-Powered Automation can streamline your Trial Master File Management.
Keeping Up With ClinOps: Why And How To Improve Delivery
Industry experts discuss the concept of a trial platform as a service and how it can accelerate and enhance the day-to-day functions of clinical operations throughout the entire lifecycle of a study.
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.
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.
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...
Enhancing Oncology Clinical Trials Through The Use Of Digital Technologies
The most difficult clinical research just became more challenging. Learn tactics on how teams can simplify oncology research while solving new and old issues.
Is It Worth The Effort To Switch To Veeva's EDC?
Kronos Bio discusses how their oncology biotech switched to Vault EDC for faster, more flexible builds.
The Medable Platform: Deep Evidence Generation
Discover how Medable's platform technology enabled a top vaccine developer to accelerate study deployment and recruitment timelines.
Document Processing: A New Hope
Tired of slow, error-prone document processing? Discover how top companies are boosting speed and accuracy while slashing costly rework. Watch now to learn how you can achieve TMF excellence faster.
Sanofi Reshapes Patient Experience With Digital Technologies
Sanofi has adopted a Patient Informed Research And Development model within the organization. The goal of the model is to work with patients, patient groups, and patient communities to understand the concerns of patients and ensure those voices are heard throughout the co...
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.
Implementing Your eCOA For Optimal Clinical Trial Success
See how having the right tools to build intuitive and patient-friendly eCOA solutions can simplify the trial experience's inherent complexity, reduce participation burden, and drive engagement and compliance.
Game On! Strategies For Conquering The Final Boss: TMF Close-Out
Much like playing a lengthy and challenging video game, managing the TMF from set-up through close-out can be an epic journey. Ever wondered how to ensure you're well-prepared to face the final boss?