Webinar Wednesdays - Clinical Research Management and Regulatory Science
Webinar Wednesdays is a monthly webinar series designed to increase the visibility of the Clinical Research Management and Regulatory Science graduate programs and contribute to the research community by providing educational opportunities to students and research professionals. This webinar offers presentations on current practices, best practices, and current thinking and knowledge by experts in the field. Webinars are from 6:00 pm - 7:00 pm every third Wednesday of the month (excluding June, July, and December).
To be added to the Webinar Wednesdays' email distribution list, which includes information on participating in the live webinars, please email Kaushal Shah at kpshah8@asu.edu.
Previous CRM Webinars
| Date | Presenter | Presentation Title |
|---|---|---|
| September 20, 2023 | Amit Algotar & Kalpana Algotar | Role of AI in Clinical Research and Clinical Care |
| March 16, 2022 | Christine Samara | Competencies of Clinical Research Professionals |
| February 16, 2021 | Professor Barb Marusiak & Capstone Student Cheryl Calhounn | Experiential Learning: Capstones and Internships |
| January 19, 2021 | Dean Chiarelli | |
| December 2021 | No Webinar | |
| October 20, 2021 | Jovelyn Harmon | |
| September 15, 2021 |
Kimberly Kelly |
Presentations by Clinical Research Management Capstone Students |
| May 19, 2021 | Dr. Clare Elser | |
| April 21, 2021 | No Webinar | |
| March 17, 2021 | Dr. Orin Chisholm | |
| November 18, 2020 | Molly Downhour | |
| Oct 21, 2020 | John Rizk | COVID-19 and the US response by pharma in accordance with regulations |
| Sep 16, 2020 | Christine Chalhoub Christine R. Thompson |
Public’s Knowledge, Perception of and Attitude towards Clinical Research in Lebanon Solving the injustices of the 510(k) Medical Device Approval Pathway by Regulating Device Genealogy, Material, and Classification |
| Jan 9, 2019 | Loretta A. Rome | Dealing with Difficult Subjects in Clinical Trials |
| Feb 27, 2019 | Ellen G. Feigal | From Consent to Medical Care to Consent to Research |
| Mar 13, 2019 | No webinar | |
| Apr 10, 2019 | Clare Elser | Data Integrity: Healthcare, AI, and Machine Learning |
| May 8, 2019 | No webinar | |
| June 12, 2019 | Ronald Harning | Recent Advances in Oncology Lead to Fewer Oncology Patients |
| 1/11/2017 | Debra King | Clinical Trial Monitoring: Historical, Future and Personal Perspective |
| 2/8/2017 | Chris Abley | Public & Patient Engagement (PPE) in clinical research - A UK perspective |
| 3/8/2017 | Barbara Marusiak | Critical Elements of Study Setup: the Sponsor |
| 4/12/2017 | Tina Escobedo | Cultural Sensitivity in Clinical Research |
| 5/10/2017 | Cris Wells | The Evolving and Emerging Clinical Research Workforce |
| 6/14/2017 | Barbara Marusiak | Critical Elements of Study Setup: the Site |
| 8/9/2017 | Maureen Martin | Quality Control (QC) of Clinical Study Report Safety Narratives and General Regulatory Submission Documents |
| 9/13/2017 | Kaushal Shah | Conducting Clinical Trials in India |
| 10/11/2017 | Mindy Bowers | Workload Management in Clinical Trials |
| 11/8/2017 | Sandy Shire | TBD |
| 1/10/2018 | Ali Rajea | Dietary Supplements Part 1 |
| 2/14/2018 | JoAnn Pfeiffer | Strategies to Reduce Time |
| 3/14/2018 | Maureen Martin | What is Drug Safety and What Opportunity Awaits in this Profession? |
| 4/11/2018 | No webinar | |
| 5/9/2018 | Ali Rejaei | Dietary Supplements Part 2 |
| 6/13/2018 | Ronald Harning | Intro to Basic Statistics and Probability in Research |
| 7/11/2018 | Orin Chisholm | A Look at Global Regulatory Affairs |
| 8/8/2018 | Maureen Martin | Career options for RNs in clinical research |
| 9/12/2018 | Loretta Rome | Increasing Retention Through Motivational Interviewing During Subject Screening |
| 10/10/2018 | Adair Turner | FDA Regulatory eSubmissions |
| 11/14/2018 | JoAnn Pfeiffer | Study Site, Sponsor Budget & Contract Strategies |
| Dec, 2018 | No webinar | |
| 4/13/2016 | Jian Wang , M.D. CEO BioFortis |
Precision Medicine - Impacts on Biobanking, Patient Informed Consent Management and Clinical Trials |
| 5/11/2016 | Jeffrey A. King, JD | Bioethics, Health Care Consent, Patient Autonomy and Surrogate Decision-Makers |
| 6/8/2013 | Clare Elser Quality Product Leader Biologics, Genentech |
Combination Products - new cGMP requirements, 21 CFR Part 4 |
| 7/13/2016 | Kathy Kenny, DNP Assistant Dean, CONHI |
Innovation: Creating Change |
| 9/14/2016 | Betsy Fallen BAFallen Consulting, LLC |
Electronic Investigator Site File: Digital Storing of Documents for Inspection Readiness |
| 10/12/2016 | Melanie Flores Director of Compliance INTEG REVIEW IRB |
Changes to the Common Rule |
| 11/9/2016 | Marilyn Windschiegl, JD Contracts and Compliance Manager PFS Clinical |
Clinical Trial Contracts 101 |