Course "Clinical Data Management" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.
Overview:
When new drugs or devices are tested in humans, the data generated by, and related to, these trials is known as clinical data. This data represents a huge investment by the biopharmaceutical or device company and is one of its greatest assets. It is this data that will eventually make a new product both useful as a treatment or therapy and marketable. The management of clinical data, from its collection during a trial to its extraction for analysis, has become a critical element in the steps to prepare a regulatory submission and to obtain approval to market a treatment. As its importance has grown, clinical data management (CDM) has changed from an essentially clerical task in the late 1970s and early 1980s to the highly computerized specialty it is today.
This seminar is based on the current state of regulations and will cover the essential parts of the data management plan, study startup, study conduct, study closeout and study monitoring.
A data management plan or DMP is a formal document that outlines how data are to be handled both during a research project, and after the project is completed. The goal of a data management plan is to consider the many aspects of data management, metadata generation, data preservation, and analysis before the project begins; this ensures that data are well-managed in the present, and prepared for preservation in the future.
Study startup activities include designing case report forms (CRFs), paper or computer; specifying cleaning rules (edit checks); building and testing the database; and releasing the study database to collect data.
Study conduct activities include collecting the data on CRFs and via electronic files, cleaning that data, managing adverse event and serious adverse event collection, and producing reports.
Study closeout focuses on ensuring the data is complete and of a quality to support final analysis.
Study monitoring is an in-person evaluation carried out by sponsor personnel or representatives at the sites at which the clinical investigation is being conducted. On-site monitoring can identify data entry errors (e.g., discrepancies between source records and case report forms (CRFs)) and missing data in source records or CRFs; and assess compliance with the protocol and investigational product
At the end of this class attendees will be able to:
Define best practices as they apply to CDM processes
Describe CDM processes from study start-up to database lock
Apply best practice rationale when assessing data collection requirements/instruments
Evaluate the benefits of standardization in establishing CDM processes
Discuss current technology/methods of data collection and associated documentation
Who Will Benefit:
New or aspiring Clinical Data Managers
Clinical Data Managers
Data Coordinators
Clinical Research Associates
Data Management Personnel
Biostatisticians
Regulators
Doctors
Nurses
Project Managers
Government employees at clinicaltrials.gov
College Students and New Graduates in a Scientific Field
This course is also ideal for "on-boarding" of individual new hires or entire teams
Agenda:
Day 1 Schedule
Lecture 1 (90 Mins):
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,
Lecture 2 (90 Mins):
Elements in Developing a Data Management Plan
Choosing vendors 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
Lecture 3 (180 Mins):
Study Startup
Essential documents
Prior to Study Commencement
During Conduct of the Trial
After Completion/Termination of the Trial
CRF design and development (paper/e-CRF)
Database build and testing
Edit Checks preparation and testing
Day 2 Schedule
Lecture 1 (90 Mins):
Study Conduct
Data Entry
External Data integration and reconciliation
Discrepancies, errors, corrections
Data Cleaning (preparation) and Coding
Lecture 2 (90 Mins):
Study Conduct (cont'd)
(MedDRA and WHODDE dictionaries)
Severe adverse events (SAE) status reporting
Data Review and Quality Control
Data Transfer procedures
Lecture 3 (90 Mins):
Study Closeout
SAE Reconciliation
Quality Control
Database Lock
Electronic Archival
Database Transfer
Enhancing Reproducibility
Lecture 4 (90 Mins):
Monitoring Visits
What to expect during a monitoring visit
Elements for Establishing a Corrective Action Plan
Jeopardy Quiz - Clinical Data Management
Speaker
Angela Bazigos
CEO, Touchstone Technologies Silicon Valley
Angela Bazigos is the CEO of Touchstone Technologies Inc. and has 40 years of experience in the Life Sciences, Healthcare & Public Health Services. She has extensive experience in Computer Systems Validation and Data Integrity including having collaborated with FDA on prototyping 21 CFR 11 in 1992-1995, patent on using virtualization to speed up validation and a book on computerized systems in clinical research co-authored with FDA and DIA . She has successfully completed 56 large validation projects with a 94% on-time / on budget record.
Location: New Orleans, LA Date: August 30th & 31st, 2018 and Time: 9:00 AM to 6:00 PM
Venue: WILL BE ANNOUNCED SOON
Price:
Price: $1,295.00 (Seminar Fee for One Delegate)
Register for 5 attendees Price: $3,885.00 $6,475.00 You Save: $2,590.00 (40%)*
Register for 10 attendees Price: $7,122.00 $12,950.00 You Save: $5,828.00 (45%)*
Register now and save $200. (Early Bird)
Until July 20, Early Bird Price: $1,295.00 From July 21 to August 28, Regular Price: $1,495.00
Sponsorship Program benefits for seminar
For More Information- https://www.globalcompliancepanel.com/control/sponsorship
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