It is no surprise that 66% of top 50 Pharma companies are engaged with or planning an eConsent initiative in the near future, with 10 of the top 10 already having a strategy in place.

To benchmark current eConsent use, gauge experiences and expectations, better understand adoption hurdles and challenges, and to anticipate how eConsent use will grow in the future, CRF Health conducted our first-ever State of eConsent Industry Survey.

146 respondents from 100 biotech, pharmaceutical, CRO, and IRB organizations have shared their opinions. In this upcoming live webinar “Electronic Informed Consent: 2017 Industry Survey Results”, we invite 30-year industry expert Sandra “Sam” Sather to discuss these findings and provide commentary.

Whether your organization is just starting to consider eConsent or looking to expand adoption company-wide, register for this free webinar to learn what others in the industry are currently thinking about the informed consent process.

Keywords:

eConsent

Speakers

Sam Sather, Quality and Regulatory, TrialConsent,CRF Health

Sam’s current focus of consulting is to promote clinical quality systems for Sponsors/CROs, Investigators and clinical research institutions. She has over 30 years of clinical experience, a Bachelor of Science degree in Nursing and a Master of Science degree in Education with a Specialization in Training and Performance Improvement.

Sam has served many roles in clinical research, including site study coordinator and manager, sponsor and CRO monitor, quality assurance auditor, risk manager, trainer, and performance management consultant. She has held clinical research industry certifications for over 15 years by the Association for Clinical Research Professionals (ACRP). SAM is a current member of the ACRP Academy Board of Trustees, and Regulatory Affairs Committee (RAC). She is a frequent subject matter expert for GCP regulation and speaker at industry conferences. Sam has authored dozens of competency based curriculums for various clinical research stakeholders.

Message Presenter

Naor Chazan, Director of Marketing, CRF Health

Naor leads the global marketing team at CRF Health and is passionate about developing educational content to help our customers excel at planning, deploying and managing their clinical trials. He has been a B2B marketer for 11 years, the last 6 of which have been in the life sciences industry, and holds a B.S. in Marketing from Rutgers Business School, along with a Marketing Strategy Certification from Cornell University.

Message Presenter

Who Should Attend?

Clinical operations
Data management
Clinical Innovation
Medical Director/Clinical Sciences
Patient Recruitment
Academic research
Clinical site management
Executive Leadership
Health Economics
Outcomes Research
Regulatory/Risk Management
Quality Assurance
Outsourcing/Vendor Relations/Procurement
Adherence and Compliance

Xtalks Partner

CRF Health

CRF Health is the leading provider of patient-centered eSource technology and service solutions for the life sciences industry. With experience in more than 800 trials, over 100 languages and across 74 countries, CRF Health’s TrialMax® platform consistently demonstrates the industry’s highest data accuracy, patient and site compliance, and patient retention.

CRF Health’s eSource solutions improve trial engagement by fitting into the lives of patients and seamlessly integrating into sites to maximize protocol compliance. The integrated TrialMax® platform includes eCOA solutions for collecting PROs (Patient Reported Outcomes), ObsROs (Observer Reported Outcomes), ClinROs (Clinician or Rater Reported Outcomes), and PerfOs (Performance Outcomes), and features TrialConsent™, an electronic solution for collecting informed consent in clinical trials.