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Best Practices for Leveraging eClinical Systems for Study Startup


Date: December 17, 2014 (60 minutes)

Featured Speakers:
  • Eldin Rammell, Managing Director and Principal Consultant, Rammell Consulting
  • Rob Wynden, VP of Technology and Engineering, goBalto

Clinical study teams, and the IT groups that support their clinical operations, have access to a variety of eClinical systems (e.g. eTMF, CTMS, and other systems). Any one, or a combination of these, can be used to manage study startup documents and activities, as well as potentially drive process improvements and shorten overall timelines. However, without a clear understanding of the best uses of each eClinical system, it's difficult to implement a solution that helps teams maximize collaboration, effectively manage document lifecycles, track metrics, and ensure compliance.

Join the webinar to discover future trends, assess available options, and implement an eClinical system that works best for your organization's particular business requirements.

Featured speakers include Eldin Rammell, records management consultant and eTMF thought leader, and Dr. Rob Wynden, VP of Technology and Engineering for goBalto, an expert in biotech feasibility, subject identification, and study startup.

Keywords: eClinical systems, Study startup, Process improvement


Eldin Rammell, Managing Director and Principal Consultant, Rammell Consulting

Eldin Rammell has over 25 years experience in the field of records management. His goal is to help organizations improve working practices, processes, and systems through the better use of information assets (records management can be a pivotal factor in achieving these improvements).

He is a frequent speaker at industry conferences including Records Management Society, MHRA Symposia, InfoTech Pharma, DIA, European Forum for Good Clinical Practice (EFGCP), CBI, ExL-Pharma, and Applied Clinical Trials. Eldin was a guest lecturer at City University, London and 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.

Rob Wynden, VP of Technology and Engineering, goBalto

Rob Wynden has been a computer scientist and programmer for 28 years in the scientific programming, e-commerce, biotech, and health care industries. He implemented study startup and CTMS functionality at nine 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.


  • Clinical Operations management and IT professionals who work in clinical study startup


We develop next-generation solutions that simplify and accelerate clinical study startup in the pharmaceutical, biotechnology, and medical device industries. Our management team has over 100 years of combined experience in the life sciences industry and enterprise software implementation. Our team has worked for such companies as Amgen, Genentech, Quintiles, Roche, Johnson & Johnson, and Model N.

We’ve been recognized as a 2013 Top 10 Biotech Techie by FierceBiotechIT, were selected as a finalist in Red Herring’s Top 100 North America Award, and received a Special Recognition Award by Partnerships in Clinical Trials. According to FierceBiotechIT, our company is recognized as “combining the best of high technology and biotechnology to solve major problems in healthcare.”

With a proven commitment to customer success, disruption, and study startup optimization, we’re changing the way our leading global pharma and CRO customers approach their business processes. Based in San Francisco, California, we have satellite offices in Pennsylvania and Singapore.

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