Clinical data management (CDM) is paramount for a successful research. After all, Garbage In, Garbage Out (GIGO).
CDM involves all aspects of collecting, processing, and interpreting information. There are many types of computer applications and database systems to support data collection and management. However, there are elements of CDM that apply across the board.
Review and approval of drugs or devices by regulatory agencies require the assumption that the data presented are valid and reliable. The integrity of the data is paramount to ensure confidence in the results and conclusions you will make.
This seminar is based on FDA E6 GCP Guidelines which are the basis of effective data quality management. Even if your research is not FDA regulated, the information you learn in this course will help to ensure a robust data collection and management plan.
The information conveyed in this course will also assist investigators in setting up processes for smoother data monitoring and auditing.
Examples of CRFs and required documentation will be presented. Data collection and preparation techniques will also be demonstrated. Additionally, this workshop will provide you with the knowledge and tools needed to assure a CDM plan that holds up when the inevitable deviations from protocol occur.
- Regulatory guidelines for Clinical Data Management
- Best practices for data collection
- Responsibilities of personnel
- Case report form criteria
- Maintaining confidentiality of data
- Data storage and transferability
- Data preparation and quality assurance for accuracy
- Data monitoring plan criteria
- Data systems validation
- Adverse event reporting and coding criteria
- What to expect on a monitoring visit
- Troubleshooting and resolution of deviations from the plan
Day 01 (8:30 AM - 4:30 PM)
8:30 - 8:59 Registration Meet & Greet.
9:00 - 10:30 Introductions: Seminar objectives review, expectations and scope.
Session 1: CDM: The Reasons and The Requirements
- GIGO = Garbage In, Garbage Out. Why we need good practices in data management
- Presentation and overview of FDA GCP Guidelines on data management
- NIH Policy (SOP 15, 17, 19)
- 21 CFR Parts 11, 312.62, 812.140
10:30 - 10:45 Break
10:45-12:00 Session 2: Elements in Developing a Data Management Plan
- Choosing a vendor and outsourcing
- Data privacy and protection of subject data
- Quality Assurance and Quality Control
- Monitoring and auditing of data
- Handling Errors and Corrections
- Storage and Transfer of Data
1:00-2:30 Session 3: Study Set-Up
- Prior to Study Commencement
- During Conduct of the Trial
- After Completion/Termination of the Trial
2:30 - 2: 45 Break
2:45-4:30 Session 4: Study Set-Up (continued)
- CRF design and development (paper/e-CRF)
- Database build and testing
- Edit Checks preparation and testing
Day 02 (8:30 AM - 4:30 PM)
9:00 -10:30 Session 1: Study Conduct
- Data Entry
- External Data integration and reconciliation
- Discrepancies, errors, corrections
- Data Cleaning (preparation) and Coding
10:30 - 10:45 Break
10:45-12:00 Session 2: Study Conduct (cont'd)
- (MedDRA and WHODDE dictionaries)
- Severe adverse events (SAE) status reporting
- Data Review and Quality Control
- Data Transfer procedures
1:00-2:30 Session 3: Study Closeout
- SAE Reconciliation
- Quality Control
- Database Lock
- Electronic Archival
- Database Transfer
- Enhancing Reproducibility
2:30 - 2:45 Break
2:45-4:30 Session 4: Monitoring Visits
- What to expect during a monitoring visit
- Elements for Establishing a Corrective Action Plan
- Question and Answer Session
Elaine Eisenbeisz is a private practice statistician and owner of Omega Statistics, a statistical consulting firm based in Southern California. Elaine has over 30 years of experience in creating data and information solutions for industries ranging from governmental agencies and corporations, to start-up companies and individual researchers.
Elaine's love of numbers began in elementary school where she placed in regional and statewide mathematics competitions. She attended University of California, Riverside, as a National Science Foundation scholar, where she earned a B.S. in Statistics with a minor in Quantitative Management, Accounting. Elaine received her Master's Certification in Applied Statistics from Texas A&M, and is currently finishing her graduate studies at Rochester Institute of Technology. Elaine is a member in good standing with the American Statistical Association as well as many other professional organizations. She is also a member of the Mensa High IQ Society. Omega Statistics holds an A+ rating with the Better Business Bureau.
For more information about this conference visit https://www.researchandmarkets.com/r/3kn1up