management

Manhica Health Research Center

Clinical data are data generated when drugs or devices are tested in humans. 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
treatment1
This course aims at training the data managers on procedures and requirements for
clinical data management, divided into the three categories: study startup, study conduct, and study closeout

Additional info

Expectations and Goals
It is expected that after this course, the trainees will have knowledge of the procedures and their
chronological order, and the regulatory requirements for clinical data management.

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Teresa

Other
Maputo

Key Information

Month(s) of trainingFebruary
Duration of training< 1 week
Audience / ParticipantsPredoctoral Trainee(s)
Trainee number11-30
Complexity of TrainingIntermediate
Language(s) of instructionEnglish
Format of TrainingHybrid (Online and In-person)
Training Location (Institution Type)Not Applicable
Program - EnrollmentOpen to any applicant globally
Cost StructureFee for Institutions
Certification or DegreeCertificate Granting Course
Application DeadlineSeptember
Planned Dates3rd of February
Cost in USD102
Grants Availableno
Research SkillsBasic research strategies and design
Research Study DesignCorrelational (e.g., case-control study, observational study--cohort, cross sectional)
Research ApproachCommunity-Based Participatory Research (CBPR)
Research MethodologyMixed and Multiple Methods
Research InfluenceInterpersonal