DIA eLearning is Internet-based courseware that can be accessed 24 hours a day, 7 days a week. Modules do not have to be taken in one sitting; users can start/stop at any time and begin where they left off. After a module is completed, users will be able to review the module for one year from the date of purchase.

Continuing Education credits are offered for some modules. To obtain Continuing Education credit (if applicable) for a module, you must receive a passing score on the exam and complete the evaluation within one month of completing the module. 

How to Access eLearning Modules

DIA has partnered with Kaplan EduNeering to provide the following eLearning modules:

Clinical Pharmaceutical eLearning Program

Tour of FDA Tour of Health Canada Tour of Health Europe Aspects of Regulatory History Bioresearch Monitoring Program (BIMO): Introduction Clinical Development Process: Investigational Product, Plan and Data Management Clinical Trial Audits and Consequences of Noncompliance Drug Safety & Adverse Event Reporting Ethical Review Boards Ethics as the Foundation to Clinical Research European Union Clinical Trials Directive Good Clinical Practices (GCPs) for New Product Investigations Good Laboratory Practices (GLPs) GxPs HIPAA-The Impact on Clinical Research Investigational Product Development Laboratory Specimens for Clinical Research Overview of the Clinical Research Process Protection of Human Subjects in Clinical Trials Selecting and Managing Clinical Contract Research Organizations (CROs) DIA's Informed Consent

Clinical Medical Device eLearning Program

Tour of FDA Tour of Health Canada Tour of Health Europe Aspects of Regulatory History Bioresearch Monitoring Program (BIMO): Introduction Clinical Development Process: Investigational Product, Plan and Data Management Ethical Review Boards Ethics as the Foundation to Clinical Research European Union Clinical Trials Directive Good Clinical Practices (GCPs) for New Product Investigations Good Laboratory Practices (GLPs) GxPs HIPAA-The Impact on Clinical Research ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials Laboratory Specimens for Clinical Research Medical Device Safety Reporting Overview of the Clinical Research Process Protection of Human Subjects in Clinical Trials Selecting and Managing Clinical Contract Research Organizations (CROs) DIA's Informed Consent

GMP Pharmaceutical eLearning Program

GxPs Orientation to GMP Compliance Biotechnology: An Overview of Compliance Considerations GMPs for API Bulk Manufacturers GMP Principles of SOPs Principles of Good Documentation Part 11-Electronic Records and Electronic Signatures Key Concepts of Process Validation Change Control Awareness of FDA Inspections for Pharmaceutical Manufacturers GMP Updates-Enforcement Changes at the New FDA Introduction to GMPs Understanding Postapproval Changes

Validation and Part 11 Compliance

Computerized Systems Inspections in the Pharmaceutical Industry Computerized Systems Inspections in the Medical Device Industry Part 11: Electronic Records and Electronic Signatures Part 11: Electronic Records and Signatures-Application