Clinical Trials Foundations and Best Practices Training-Day 1
Date: Apr 17, 2026 09:00 AM - 01:00 PM
Fee
$0.00
CE Hours
3.25
CE Units
0.325
Registration closes on Apr 30, 2026 10:00 PM
Activity Type
- Knowledge
Target Audience(s)
- Pharmacists
Accreditation(s)
Accreditation Statement: Howard University College of Pharmacy is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education.
Objectives
- Describe a historical perspective of human research.
- Identify the proceedings that shaped the evolution clinical research
Speaker(s)/Author(s)
|
Celia J. Maxwell, MD |
Date:
04/17/26
Time:
09:15 AM - 10:15 AM
CE Hours
1.00
Objectives
- Define the role of the regulatory bodies (FDA, OHRP, ICH).
- Describe the role of the guidelines (ICH E6, CFR, Part 312).
- Define the role of IRBs.
Speaker(s)/Author(s)
|
Edward Bauer |
Date:
04/17/26
Time:
10:15 AM - 10:50 AM
CE Hours
0.50
Objectives
- Classify the clinical trial phases and objectives.
- Outline the study designs of landmark studies.
- Recognize the responsibilities of sponsors, investigators, and staff.
- Outline the importance of training and delegation of tasks.
Speaker(s)/Author(s)
|
Sarah Shami, Pharm.D. |
Date:
04/17/26
Time:
10:50 AM - 11:30 AM
CE Hours
0.50
Objectives
- Identify the responsibilities of sponsors, investigators, and study staff in clinical trials.
- Explain the importance of proper training and delegation of tasks in conducting clinical research.
Speaker(s)/Author(s)
|
Sarah Shami, Pharm.D. |
Date:
04/17/26
Time:
11:30 AM - 11:45 AM
CE Hours
0.25
Objectives
- Define the key elements and process of informed consent, including considerations for vulnerable populations.
- Recognize the importance of accurate data collection, including source documents and Case Report Forms (CRFs).
- Identify practices to ensure data security and confidentiality in clinical research.
Speaker(s)/Author(s)
|
Edward Bauer |
Date:
04/17/26
Time:
11:45 AM - 12:20 PM
CE Hours
0.50
Objectives
- Describe the importance of accurate data collection and documentation in clinical research.
- Recognize the role of source documents and Case Report Forms (CRFs) in data management.
- Identify methods to ensure data security and participant confidentiality..
Speaker(s)/Author(s)
|
Edward Bauer |
Date:
04/17/26
Time:
12:20 PM - 12:50 PM
CE Hours
0.50