Presenters: Shannon Roznoski, CCDM, Director, Product Management, Forte; Stuart Cotter, Product Manager, Forte
Watch this webinar to hear our expert presenters provide an overview of 21 CFR Part 11 and discuss the roles both organizations and vendors play during the validation process.
Wendy Tate, PhD, MS, Director of Analytics, Forte
During this webinar, Forte's Director of Analytics, Wendy Tate, outlines essential factors of effective clinical trial project management and provides tips to help you successfully manage your individual research portfolio.
Shanley Curran, JD BSN CHRC CHC CCRP, Founder & CEO, Research, Operations & Compliance Solutions, Inc.
During this webinar, you'll learn steps for operationalizing your coverage analysis across critical points of communication to achieve the billing, correct claims, and full reimbursement goals it drives.
Presenters: Shannon Labout, CCDM, Interim Chief Standards Officer / VP of Education, Clinical Data Interchange Standards Consortium (CDISC); Shannon Roznoski, CCDM, Director, Product Management, Forte
Join us for this free webinar to hear Shannon Labout of CDISC and Shannon Roznoski of Forte explore the value of quality data in clinical trials and the necessary skills for effective data management.
Christina Brennan, Vice President of Clinical Research, Northwell Health
During this webinar, Christina Brennan of Northwell Health discusses the benefits of centralizing research operations by establishing a central clinical trials office.
Presenters: James Wurdeman, Senior Vice President, Products & Quality, Forte; Kate Fiorito, IT Clinical Research Systems Analyst, Fox Chase Cancer Center - Temple Health; Brian Sevier, Director, Office of Clinical Research, University of Florida; Ray Skeps, Clinical Research Protocol Review System Manager, Fred Hutchinson Cancer Research Center
Hear our expert panelists discuss their predictions for clinical research in the coming year. Discover insights on centralization of research operations, the push for more electronic solutions, adapting to changes in national standards, the growing complexity of modern trials, and much more.
Presenters: Bishoy Anastasi, Director, Office of Clinical Research, University of California, Los Angeles (UCLA); David Goodrich, Assistant Director, Office of Clinical Research, Indiana University (IU)
During this webinar, Bishoy Anastasi of UCLA and David Goodrich of IU will discuss how their respective organizations addressed common challenges in financial management processes.
Presenters: Beth Harper, President, Clinical Performance Partners, Inc.; Kelly Anastasio, Associate Director of Clinical Trial Resources, Yale University
During this presentation, expert panelists will discuss common challenges and potential solutions to improve patient recruitment in clinical trials.
Presenters: Wendy Tate, PhD, MS, Director of Analytics, Forte; Mariette Marsh, MPA, CIP, Director of the Human Subjects Protection & Privacy Program University of Arizona
During this presentation, you’ll learn how to maintain ethical delegation of authority, strategies for institutional process improvement & more.
View this on-demand webinar where Forte's Regina Schwind will discuss how recent updates to the CCSG guidelines impact your research practices.