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2020 Webinar Events  

As more people are working from home during COVID-19,¬† it’s more important than ever to stay connected and on top of how Clinical Trials are changing in the wake of the pandemic.¬† We are scheduling a series of webinars around various topics, many focused on sharing information about the impact of COVID-19 on current and future clinical trials. Please register in advance for all webinars as space is limited.

SureQMS smart QMS

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‚Äôs.

Using Game Design to Improve Clinical Trials

Please join us at an exciting and educational webinar where our guest speaker, Olli Rundgren, CEO of Psyon Games, will share how his lifetime fascination with games and poker, where he was a high stakes player, led him to create a platform that helps Pharma and Biopharma companies market their products, at the same time collecting audience demographics, attitudes and behaviour patterns. 

Psyon Games is the Winner of the 2020 Eyeforpharma/Reuters Health Start-Up Challenge – the first-ever game company to win the title.

We’ll show you how this approach increases subject enrollment, compliance and improved change management through your eClinical landscape as well.

How to Survive a TMF Audit - A View from an Auditor

Do the words “eTMF Audit” spark joy?  For most Sponsors and CRO‚Äôs, 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

Join us on this webinar where our guest speaker Maria Kuthning, who spent the last 6+ years as Head of Global Clinical trial Systems at Boehringer Ingelheim, shares her insights and predictions of how COVID-19 will affect clinical trial management in the future and the need to securely digitalize trials. 

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 SureClinical and 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

Join SureClinical and 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 SureClinical and 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.

 Best Practices for Study Startup: Leveraging Digital Signatures and Process Automation

Clinical trial study startup processes are an area ripe for optimization. Often, the study time clock doesn’t start ticking until First Patient In (FPI), but research shows that the process to get to FPI can take seven months or longer on average.This webinar explores best practices for study startup with practical advice on how to reap the benefits of automating processes while increasing compliance. The featured speakers discussed common misconceptions around digital versus electronic signatures and provide advice on how to ensure all of those signed documents comply with US Food and Drug Administration (FDA) 21 CFR Part 11 guidance.

2020 Conferences

Due to Covid-19 restrictions, we are unable to meet you in person as originally planned for in 2020.  We look forward to seeing you at future conferences.  We are starting to participate in virtual events, which are proving to be very beneficial, so we hope to see you all soon virtually. Also, please subscribe to our webinar series to stay in touch and learn the latest trends in digital clinical operations management.

Visit our booth during the event for a demo or just to say hello. 

November 2-4, 2020 – Virtual

Contact us to schedule a demo or meeting.

Contact us to schedule a demo or meeting.

2020 Lunch and Learn Events

Turbocharge your Clinical Trials!  

Are clinical trial startup processes taking too much time? Research shows that clinical site initiation times can take 7 months or longer on average. 

Contact us today to learn more about our 2020 eClinical Lunch & Learn series where you can network with peers and learn how others in the industry are helping their companies save time, save costs, enhance quality and accelerate project milestone delivery.