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Event Cost:
1699
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Event Capacity
20
For registration/tickets purchase:
https://www.complianceonline.com/clinical-data-management-cdm-seminar-training-80552SEM-prdsm?channel=medicalevents
Notable Speakers
Elaine Eisenbeisz
Session brief description
Clinical Data Management (CDM) 2020 California United States
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Session End Date
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Brief Description

Clinical Data Management (CDM) 2020 California United States

Clinical data management (CDM) is paramount for 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.

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
Abstract Submission Deadline
Abstract guidelines

Clinical Data Management (CDM) 2020 California United States

Clinical Data Management (CDM) 2020 Caliornia United States

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.

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

Contact Organizer

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Country: United States     City: Caliornia
(1+) 206-575-7771
World Medical Events Company
12922 SE 299th Street, Auburn WA 98092 USA