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With the move to remote monitoring, digital data and AI, it’s more important than ever to stay connected and on top of how Clinical Trials are changing. Schedule a meeting with us today to learn more.
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 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.