Good Clinical Data Management Practices (GCDMP)


Starting at

$1699

Premier pro price: $1614 (save 5%)

Buy Now

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 requires the assumption that the data presented are valid and reliable. 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 CRF’s 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.

Learning Objectives:

  • 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 plan

Who will Benefit:

  • Study Investigators
  • Data managers
  • Data processors
  • Statisticians
  • Site Personnel
  • Clinical Research Associates
  • Clinical Project Managers/Leaders
  • Study Sponsors
  • Professionals in pharmaceutical, medical device, clinical and biotechnology research who oversee or work with data collection and management
  • Staff in the above fields who work with data collection/management and require training in CDM.
  • Compliance auditors and regulatory professionals who require a knowledge of CDM in assessment of study protocols and reports
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
  • 12:00-1:00 Lunch
  • 1:00-2:30 Session 3: Study Set-Up
    • Essential documents
      • 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 dictionaires)
    • Severe adverse events (SAE) status reporting
    • Data Review and Quality Control
    • Data Transfer procedures
  • 12:00-1:00 Lunch
  • 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
Seminar (Price/Register)
Seminar Fee Includes:
Lunch
AM-PM Tea/Coffee
Seminar Material
Attendance Certificate
$100 Gift Cert for next seminar

Other Registration Option
  1. Download the Order Form
  2. Fill this form with attendee details & payment details
  3. Fax your PO to 1-888-883-7697 or,
  4. Email it to cs@compliance.world

Payment Mode

By Check -

Pay your check issued from the payee to "Redstone Learning Inc." (Our Parent Company) and mail the check to –
Compliance.world (Redstone Learning Inc.)
1180 Avenue of the Americas,
8th Floor, New York,
NY 10036

  Media Partners

If you wish to partner with us for this event

please contact us: partner or
call us: 1-866-978-0800

Media Partner Benefits

  • Logo and company data on the event website.
  • Logo on the conference material distributed during the conference.
  • Media Partner’s brochure distributed along with conference material.
  • Logo on all the mailings before and after the event.
  • 10% discount to media partner's subscribers.

Media Partner to do

  • Banner (min 728x90 or 468x60) on the Media Partner website.
  • Insertion of the event in the event calendar, both printed and/or online.
  • Announcement article of the conference on the Magazine and/or Website.
  • Dedicated email blast to all subscribers of Media Partner.
  • Article on the Magazine and/or Website after the conference.

  Sponsors

If you wish to partner with us for this event

please contact us: sponsor@compliance.world or
call us: 1-866-978-0800

Toll Free

1-866-978-0800

Fax

1-888-883-7697