SterlingBio Events
Events
Whether your interest is in clinical, technology or AI, it’s more important than ever to stay connected and on top of how Clinical Trials are changing. Join us for an event, webinar or conference, or just click on ‘Schedule a meeting’ to meet with us.
JP Morgan 2025 / Biotech Showcase 2025
Go Fast, Go Free with SterlingBio CRO and Private AI Solutions
Discover how SterlingBio is accelerating clinical research outcomes with our “Go Fast, Go Free” services and innovative clinical AI solutions.
Join us at the JP Morgan Biotech Showcase in San Francisco, January 13–15, 2025, to learn how we help small and midsize biopharma sponsors accelerate their trials while saving costs.
📍 Event Details: JPM Biotech Showcase, January 13–15, 2025, San Francisco, CA
Conference Facility: San Franciso Hilton Hotel, Union Square 333 O’Farrell Street San Francisco, California 94102 USA. +1 415-771-1400
🌟 What You’ll Learn and Who You’ll Meet
Learn how SterlingBio’s one-stop-shop for clinical services and AI-powered solutions delivers speed, efficiency, and value. Learn how our Sure AI platform centralizes clinical intelligence to drive smarter decision-making.
Meet key members of our executive team. To schedule an executive meeting, use the BioTech showcase partnership meeting scheduler (link below).
📅 To Schedule a Meeting or to Visit Us at JPM 2025: Register to visit SterlingBio’s display or schedule a partnering meeting at Demy Colton Biotech Showcase: https://demy-colton.com/biotech-showcase/
Video Preview: To learn more about SterlingBio’s Go Fast, Go Free event at JPM 2025, watch our one minute JPM 2025 overview video here: https://youtu.be/g49nUCQ34Uc
🔔 Subscribe! Don’t Miss Out! Subscribe to SterlingBio’s Youtube channel for updates and info on how SterlingBio is redefining clinical trials.
Webinars
New! Coming in January 2025 Augmenting Intelligence (AI) in Clinical Operations
Does the word “AI” spark fear or excitement among your clinical operations team? Learn how clinical sponsors, sites and research organizations are adopting AI for a more productive workforce. Learn how you AI can augment, not replace, your valued team members. An additional technology overview will be presented showing how a centralized clinical intelligence system can be used on a private VPN for analytics and reporting across multiple studies.
Archived Webinars and Events
Best Practices for eTMF Standards and Interoperability
Digital transformation is well underway in clinical trial management as most Sponsors and CROs are moving towards electronic Trial Master Files (eTMF) and other digital solutions to manage their trials. But, there is a learning curve to understand and ensure interoperability, eTMF data sharing and standards. This webinar will explore flexible standards-based approaches to consistently and seamlessly share your eTMF data with partners, vendors, sponsors and CRO’s.
How to Survive a TMF Audit - A View from an Auditor
Do the words “eTMF Audit” spark joy? For most Sponsors and CRO’s, the answer is usually not yes. This webinar shows how it can be relatively painless with some good preparation practices and the right digital tools in place.
Introducing SureESign Enterprise
Why is digital signing such a hot topic? When you consider how many documents need to be signed over the course of a clinical trial, the answer becomes clear. This webinar highlights the recent release of SureESign Enterprise, the independently validated FDA Part 11, HIPAA, EC Annex 11 compliant trusted digital signing solution for trusted digital signing both within and outside your organization to your own trusted private network of projects, people, partners and sites.
Digitalization in Clinical Trials: The New Normal Post COVID-19
Sponsor Oversight: COVID-19 Challenges and Solutions
The need for oversight from Sponsors and CRO’s is becoming greater than ever given what is becoming the new normal of remote and virtual trials. Join us on this webinar where Karin Koehler-Hansner, PhD, Managing Director of AH Clinical Trial Services, shares her global clinical trial experience providing quality audits and sponsor oversight into how you best provide oversight and remain audit ready in this rapidly changing clinical environment.
COVID-19 Impact on Regulatory Compliance
Join Regulatory Professionals, Inc. in a webinar and learn how Sponsors and CRO’s are adjusting to the new FDA guidance, understand necessary changes to trial protocols and engagement with IRB’s and the IEC due to COVID-19, and support virtual subject visits.
An Industry Perspective: eClinical Operations and Remote Monitoring
Meet with Clinilabs and learn how Clinilabs has pivoted quickly ongoing clinical trials and planning for new ones given updated FDA guidance and social distancing requirements. We will show a short demo of SureClinical eClinical unified suite that is being used to manage trials and stay compliant, even in the wake of our rapidly changing clinical trial environment.
Future of Clinical Trials
Managing Clinical Trials Remotely
The COVID-19 pandemic has affected all areas of our lives, and those of us in clinical trials are working to understand how we can continue to progress with ongoing trials and accelerate new ones. Join SterlingBio to explore the implications of the updated FDA guidance for trials during COVID-19, and learn how to best leverage your existing technology investment in SureClinical for remote trial management and monitoring.