Using eClinical systems to speed up clinical trials

Assess and integrate eClinical systems for best results

Fully optimizing the clinical trials process requires practices and tools that streamline operations, automate processes, increase visibility and improve collaboration with sponsors, CROs, sites, regulators and review boards. The entire clinical ecosystem needs an overhaul and today pharmaceutical companies have access to a variety of cloud-based technologies that can radically improve the clinical trials process — but which tool to use and when? The webinar will focus on study startup as it relates to the overall picture of clinical study management and the opportunities and challenges associated with implementations in the eClinical stack.

In this webinar we will explore:

  • Considerations for assessing the best eClinical tools to speed clinical trials
  • How does a study startup (SSU) solution differ from an existing CTMS or eTMF solutions?
  • Benefits to using dedicated SSU solutions
  • Opportunities and challenges to integrating with eClinical applications

This webinar is applicable to:

  • Sponsor and CRO roles responsible for site selection and activation
  • Sponsor and CRO roles responsible for collecting and evaluating performance metrics
  • Sponsor and CRO roles responsible for project management of trials initiation and systems integration

Presenters:

Rob Wynden
Rob has been a computer scientist and programmer for over 30 years in the scientific programming, e-commerce, biotech, and health care industries. He implemented study startup and CTMS functionality at 9 bay area biotech companies, and invented a method that allows medical and biotech organizations to use cloud-based analytics to monitor patient data. He holds a BS in Computer Engineering from Sacramento State University and a PhD in Biological and Biomedical Clinical Informatics from UCSF.
ROBERT WYNDEN
VP Technology and Engineering
goBalto
Eldin has over 17 years industry experience prior to becoming a consultant. In 2003, Eldin left Pfizer as Associate Director of Records Management and established Rammell Consulting to help companies and organisations improve their records management processes.

Eldin has been a speaker at conferences including Records Management Society, MHRA Symposia, InfoTech Pharma, the Drug Information Association (DIA), European Forum for Good Clinical Practice (EFGCP), CBI/Advanstar, ExL-Pharma and Applied Clinical Trials; he has been a guest lecturer at City University, London; he has published articles in the GCP Journal and Clinical Researcher. He is an Executive Committee Member and past-President of the Good Clinical Practice Records Managers Association (GCP-RMA) and Director in the Scientific Archivists Group. Learn more
ELDIN RAMMELL
Managing Director and Principal Consultant
Rammell Consulting Limited
Eldin Rammell
Doug Summe
Doug has over 10 years of experience in the building and implementation of software integrations for Enterprise SaaS applications for fortune 100 companies. His primary focus has been on REST and SAML2.0 to integrate 3rd party software, customer ESB and internal applications. Doug leads the integration of the goBalto study startup suite of applications with leading eClinical systems and holds PMP and ACP certifications from the Project Management Institute (PMI).
DOUG SUMME
Director, Project Management & Integrations
goBalto

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