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About This Webinar

Sponsored by Exostar
Pharmas, CROs, and sites all are affected by this industry-wide problem of enabling access to site facing applications, which creates undue burden on everyone. Traditional access management has resulted in unique accounts to access each clinical application or in some cases a sponsor has elected to develop their own access management portal which results in creation of yet another unique account for access to the sponsor’s set of applications.

Today’s IT advancements in the area of access management enables us to address this challenge by issuing a single account to access site facing applications across sponsors. Capabilities like delegated administration allow each sponsor to approve user access to their applications, maintaining full control of their systems.

Learn how to simplify clinical application access for your sites.

Learning Objectives:
• How to reduce the burden on end-users, administrators, and IT
• How to avoid creating new accounts during study startup
• Learn how the next IT advancement will help eliminate the password
• Learn how a single account approach can help you protect your clinical assets

Who can view: Everyone
Webinar Price: Free
Featured Presenters
Webinar hosting presenter

Kenny Kong

Director, Life Sciences & Health IT, Exostar
Serving as Exostar’s Director of Health IT & Life Sciences, Kenny has consulted and advised some of the world’s largest Healthcare and Biopharmaceutical companies in enabling on-demand access to eClinical technology. In his tenure, Kenny’s thought-leadership supported the development of Federal Health IT Standards to combat the national Opioid epidemic and co-founded a federal program that brought Health IT to medically underserved areas across the United States. Kenny is an experienced leader in the clinical implementation of technology.
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Webinar hosting presenter

Cathy Carfagno

Principle, Surf the Line Consulting LLC
Ms. Carfagno is an authority on the business processes and associated use of information technology in the end-to-end drug development process with a focus on clinical and regulatory.

Over multiple decades working in various organizations such as Merck & Co., Merck J&J Joint Venture, IMS and Prudential, both in business and IT roles she was recognized for her leadership and represented these organizations on multiple internal transformational teams and industry initiatives.

Now consulting, she is following the continuing technology Innovation adoption storyline. Dedicated to partnering with the many voices in the drug development process to continually progress towards innovation and efficiency as they surf the tech line and catch the next innovation wave and investment opportunity.

She has been a speaker/consultant at various forums:
• Chairman Industry Clinical Portal Forum
• TransCelerate Bio Pharma
• DIA Regulatory Submissions, Information, and Document Management Forum
• SCOPE Summit for Clinical Ops Executives
• Industry of Things World USA

Education: BA Business Administration; Master of Science, Masters Certificate in Technical Leadership
Specialties: Clinical Trial Management, Account, Budget, Contract and Portfolio Management
Certified: Project Management Professional (PMP), Six Sigma Green Belt (SSCGB), Change Agent Capabilities (CAC), Scrum Master (CSM)
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