Complete List of Individual Courses and Professional Certification Programs
Courses below are listed by category. We have over 300 programs available. All courses are current, include voiceovers, a final assessment, and engaging activities.
- Clinical Trials Management and Monitoring
- Computer System Validation (CSV)
- Drug Safety & Pharmacovigilance
- Electronic Records & Signatures
- Good Laboratory Practices (GLP)
- Good Manufacturing Practices
- Medical Devices
- OSHA and HR EEO
- Pharmaceutical Regulatory Affairs
- Pharmaceutical Sales and Marketing
- Validation for GxP Compliant Companies
AI Expert-in-the-Loop
|
|
![]() |
Basic Skills – AI Regulatory Compliance Management: Expert-in-the-Loop (EIL) Professional Certification ProgramCourse ID: AI-201 |
![]() |
Advanced Skills – AI Regulatory Compliance Management: Expert-in-the-Loop (EIL) Professional Certification ProgramCourse ID: AI-301 |
![]() |
Specialty Skills – AI Regulatory Compliance Management: Expert-in-the-Loop (EIL) Professional Certification ProgramCourse ID: AI-401 |
Clinical Trials Management and Monitoring
|
|
![]() |
Clinical Trials Management (US & EU) Professional Certification ProgramCourse ID: GCP00A1 |
![]() |
Clinical Research Associate (CRA) Professional Certification ProgramCourse ID: GCP00A |
![]() |
Clinical Research Coordinator (CRC) Professional Certification ProgramCourse ID: CRCPRO |
![]() |
Regulatory Affairs for Clinical Research (US & EU) Professional Certification ProgramCourse ID: GCP00A2 |
![]() |
GCP: ICH-GCP Good Clinical Practice E6(R3)Course ID: GCP001 |
![]() |
Clinical Trials: Preparation and DesignCourse ID: GCP002 |
![]() |
Clinical Trials and Drug DevelopmentCourse ID: GCP003 |
![]() |
Clinical Trial Monitoring: Site Evaluation and Set-upCourse ID: GCP004 |
![]() |
Clinical Trial Monitoring: Documentation and ClosureCourse ID: GCP005 |
![]() |
Clinical Trials: Preparing for an Audit or InspectionCourse ID: GCP006 |
![]() |
Clinical Trials: The Investigational New Drug Application (IND) to Conduct FDA-regulated Clinical TrialsCourse ID: GCP007 |
![]() |
Clinical Trials: How to Obtain Approval to Conduct Clinical Trials in the EUCourse ID: GCP020 |
![]() |
Clinical Trials: How to Gain Authorization for Clinical Research Under the EU Clinical Trials RegulationCourse ID: CT11 |
![]() |
Clinical Trials: How to Conduct Clinical Research Under the EU Clinical Trials RegulationCourse ID: CT12 |
![]() |
Good Clinical Practice Training (GCP): ICH E6(R3)Course ID: CP022a |
![]() |
Major Changes in GCP from ICH E6(R2) to (R3): Road MapCourse ID: CP023a |
![]() |
DIGR-ACT® Solution: Critical Thinking Skills – Including Root Cause Analysis & CAPACourse ID: CP001a |
![]() |
Critical Thinking for Clinical Research ProfessionalsCourse ID: CP020a |
![]() |
GCP Training: ICH E6(R2)Course ID: CP002a |
![]() |
GCP Refresher Training for the Experienced ProfessionalCourse ID: CP003a |
![]() |
ICH E6(R2) GCP Training for Investigator Site Personnel (Investigators and CRCs)Course ID: CP004a |
![]() |
Overview of ICH E8(R1): General Considerations for Clinical Studies GuidelineCourse ID: CP019a |
![]() |
Good Documentation Practices and ALCOA-CCourse ID: CP005a |
![]() |
Corrective and Preventive Action (CAPA) Process Planning for Clinical Research ProfessionalsCourse ID: CP006a |
![]() |
CRO OversightCourse ID: CP007a |
![]() |
ISO 14155:2020 Medical Device StandardCourse ID: CP008a |
![]() |
Medical Device vs. Drug: Comparing and ContrastingCourse ID: CP010a |
![]() |
Investigator Initiated Clinical TrialsCourse ID: CP011a |
![]() |
Clinical Safety Data Management: Definitions and Standards for Expedited Reporting (ICH E2A)Course ID: CP012a |
![]() |
Structure and Content of Clinical Study Reports (ICH E3)Course ID: CP013a |
![]() |
Overview of 21 CFR Part 50 Human Subject Protection (HSP) and 21 CFR Part 56 IRB/IECCourse ID: CP014a |
![]() |
Overview of 21 CFR Part 312 Investigational New Drug Application (IND) and 21 CFR 314 Application for FDA Approval to Market a New Drug (NDA)Course ID: CP015a |
![]() |
Overview of 21 CFR Part 54 Financial Disclosure & Part 11 Electronic Data SignaturesCourse ID: CP016a |
![]() |
Regulatory Requirements for Clinical Trials in Europe (Directive to Regulation)Course ID: CP018a |
![]() |
HIPAA Training for Clinical Trial ProfessionalsCourse ID: CP017a |
![]() |
The General Data Protection Regulation (GDPR) and Clinical TrialsCourse ID: CP009a |
![]() |
Clinical Trial eSystems Inspection ReadinessCourse ID: CP021a |
![]() |
GCP Refresher Training: ICH E6(R3)Course ID: CP024a |
![]() |
Clinical Trials in Drug Development (Fundamentals)Course ID: CT04A |
![]() |
Clinical Trials: Protocol Design (Fundamentals)Course ID: CT04B |
![]() |
Clinical Trials: Preparation (Fundamentals)Course ID: CT04C |
![]() |
Clinical Trials: Endpoints (Fundamentals)Course ID: CT04D |
![]() |
Clinical Trials: Statistical Elements (Fundamentals)Course ID: CT04E |
![]() |
Clinical Trials: Study Design (Fundamentals)Course ID: CT04F |
![]() |
Clinical Trials: Data Capture (Fundamentals)Course ID: CT04G |
![]() |
GCP: ICH, Harmonization, and Principles of GCP ICH E6(R3)Course ID: CT03A |
![]() |
GCP: Clinical Research Teamwork (Fundamentals)Course ID: CT03B |
![]() |
GCP: Clinical Trial GCP ICH E6(R3) Records and Data Governance (Fundamentals)Course ID: CT03C |
![]() |
GCP: Clinical Trial Sponsors GCP ICH E6(R3) Responsibilities (Fundamentals)Course ID: CT03D |
![]() |
GCP: Clinical Trial Investigators GCP ICH E6(R3) Responsibilities (Fundamentals)Course ID: CT03E |
![]() |
GCP: Informed Consent in Clinical Trials (Fundamentals)Course ID: CT03F |
![]() |
GCP: Clinical Trial Monitors GCP ICH E6(R3) Responsibilities (Fundamentals)Course ID: CT03G |
Computer System Validation (CSV)
|
|
![]() |
Computer System Validation for ProfessionalsCourse ID: VAL00S2 |
![]() |
Computer Software Assurance (CSA) Professional Certification ProgramCourse ID: CSAPRO |
![]() |
CSA: Computer Software AssuranceCourse ID: CSA-101 |
![]() |
Validation & Compliance: Commercial-off-the-shelf (COTS), Software-as-a-service (SaaS) and Cloud SystemsCourse ID: CSA-301 |
![]() |
Validation: Computer System Validation (Part 1 of 2) (Planning)Course ID: VAL09 |
![]() |
Validation: Computer System Validation (Part 2 of 2) (Implementation)Course ID: VAL10 |
Drug Safety
|
|
![]() |
Drug Safety and Pharmacovigilance Professional Certification ProgramCourse ID: AV01 |
![]() |
Pharmacokinetics and Pharmacodynamics for ProfessionalsCourse ID: AV01A |
![]() |
Good Pharmacoepidemiology Practice Professional Certification ProgramCourse ID: AV01B |
![]() |
Introduction to Drug Safety and PharmacovigilanceCourse ID: AV02 |
![]() |
Drug Safety: Signal Detection and Management in PharmacovigilanceCourse ID: PV04 |
![]() |
Drug Safety: Risk Management Planning for Medicinal ProductsCourse ID: PV05 |
![]() |
Drug Safety: Urgent Safety RestrictionsCourse ID: PV06 |
![]() |
Drug Safety: Good Pharmacoepidemiology PracticeCourse ID: PV07 |
![]() |
Safety Reporting in Clinical Trials (Adverse Event Reporting)Course ID: CT13 |
![]() |
Clinical Trial Safety Reporting Requirements in the EU and USACourse ID: CT14 |
![]() |
Introduction to Pharmacokinetics and Pharmacodynamics in Drug Development and RegistrationCourse ID: PKPD01 |
![]() |
Conducting Pharmacokinetic and Pharmacodynamic StudiesCourse ID: PKPD02 |
Electronic Records
|
|
![]() |
Compliance with Regulation 21 CFR Part 11 (Electronic Records and Electronic Signatures)Course ID: ESR01A |
![]() |
Assuring Data Integrity in the Manufacture of Medicinal ProductsCourse ID: ICT02 |
![]() |
Assuring Data Integrity in Clinical ResearchCourse ID: ICT03 |
GMP for Dietary Supplement Manufacturing
|
|
![]() |
cGMPs for Dietary Supplements (21 CFR Part 111)Course ID: GMPDS |
GMP for Food Manufacturing
|
|
![]() |
GMP: Food Manufacturing for Professionals (21 CFR Part 117)Course ID: GMPF |
![]() |
GMP Awareness: Food ManufacturingCourse ID: GMPF01 |
![]() |
GMP: Food Manufacturing Warning Letters and Case StudiesCourse ID: GMPF02 |
![]() |
GMP for Food Manufacturing: The Nine (9) Principles of 21 CFR Part 117Course ID: GMPF03 |
Good Laboratory Practices
|
|
![]() |
Good Laboratory Practice (GLP) Professional Certification ProgramCourse ID: GLPRO |
![]() |
Good Laboratory Practice (GLP)Course ID: GLP01 |
![]() |
G(QC)LP: Good Quality Control Laboratory PracticeCourse ID: GLP02 |
![]() |
Good Clinical Laboratory Practice (GCLP)Course ID: GLP03 |
![]() |
Introduction to Good Laboratory Practice (GLP)Course ID: GLP-101 |
![]() |
GLP: Stability Testing ProgramsCourse ID: GLP-401 |
![]() |
GLP: Sampling PlansCourse ID: GLP-501 |
Good Manufacturing Practices
|
|
![]() |
Current Good Manufacturing Practice (cGMP) Professional Certification ProgramCourse ID: GMP001S1 |
![]() |
GMP Refresher Program for ProfessionalsCourse ID: GMPREF |
![]() |
GxP: Good Practices (GxP) in Drug Development and ManufacturingCourse ID: GXP01 |
![]() |
Standard Operating Procedures (SOPs) in the GxP Regulated IndustryCourse ID: SOP-101 |
![]() |
Quality Risk Management (QRM ICH-Q9): Accessing Risks in Daily OperationsCourse ID: QRM-101 |
![]() |
cGMP: Introduction to Good Manufacturing Practice (GMP)Course ID: GMP01 |
![]() |
cGMP: Warehouse for PharmaceuticalsCourse ID: GMP02 |
![]() |
cGMP: Microbiology in the WorkplaceCourse ID: GMP03 |
![]() |
cGMP: Cleaning and SanitationCourse ID: GMP04 |
![]() |
cGMP: Documentation and Record Keeping (GDocP)Course ID: GMP05 |
![]() |
cGMP: Contamination ControlCourse ID: GMP06 |
![]() |
cGMP: Production ControlsCourse ID: GMP07 |
![]() |
cGMP: Packaging ControlsCourse ID: GMP08 |
![]() |
cGMP: Quality Assurance and Quality Control (QA/QC)Course ID: GMP09 |
![]() |
cGMP: Pharmaceutical Corrective and Preventive Action (CAPA) – Including Root Cause AnalysisCourse ID: GMP10 |
![]() |
cGMP: Data IntegrityCourse ID: GMP11 |
![]() |
cGMP: Introduction to Good Manufacturing Practice for Medicinal ProductsCourse ID: CGMP01 |
![]() |
cGMP: Good Documentation Practice (GDocP)Course ID: CGMP02 |
![]() |
cGMP: Good Manufacturing Practice in Cleaning and SanitationCourse ID: CGMP03 |
![]() |
cGMP: Good Manufacturing Practice for the WarehouseCourse ID: CGMP04 |
![]() |
cGMP: Good Manufacturing Practice in Processing Medicinal ProductsCourse ID: CGMP05 |
![]() |
cGMP: Good Manufacturing Practice in Packaging Medicinal ProductsCourse ID: CGMP06 |
![]() |
cGMP: Corrective and Preventive Action (CAPA) in Medicinal Product Manufacturing – Including Root Cause AnalysisCourse ID: CGMP07 |
![]() |
cGMP: What is GMP and Why is it Important (Fundamentals)Course ID: CGMP01a |
![]() |
cGMP: The Principles of GMP (Fundamentals)Course ID: CGMP01b |
![]() |
cGMP: Hygiene, Cleaning, and Sanitation (Fundamentals)Course ID: CGMP01c |
![]() |
cGMP: Documentation and Record Keeping (Fundamentals)Course ID: CGMP01d |
Medical Devices
|
|
![]() |
Introduction to the Regulation of Medical DevicesCourse ID: MDA0 |
![]() |
Quality Management System Requirements for Medical Devices under ISO 13485:2016 and FDA QMSRCourse ID: MD02 |
OSHA and EEO
|
|
![]() |
OSHA for Healthcare ProfessionalsCourse ID: OSHAPRO |
![]() |
OSHA: Bloodborne Pathogens for Healthcare WorkersCourse ID: OSHA-01 |
![]() |
OSHA: Chemical SafetyCourse ID: OSHA-02 |
![]() |
OSHA: Compressed Gas SafetyCourse ID: OSHA-03 |
![]() |
OSHA: Electrical Safety for HealthcareCourse ID: OSHA-04 |
![]() |
OSHA: Emergency Response PlanCourse ID: OSHA-05 |
![]() |
OSHA: Environmental Cleaning-Exam RoomsCourse ID: OSHA-06 |
![]() |
OSHA: Fire Safety and Emergency EvacuationCourse ID: OSHA-07 |
![]() |
OSHA: Flammable Liquid SafetyCourse ID: OSHA-08 |
![]() |
OSHA: Formaldehyde SafetyCourse ID: OSHA-09 |
![]() |
OSHA: Hand HygieneCourse ID: OSHA-10 |
![]() |
OSHA: Hazard Communications for HealthcareCourse ID: OSHA-11 |
![]() |
OSHA: Incident Reporting in HealthcareCourse ID: OSHA-12 |
![]() |
OSHA: Infection Control for Healthcare ProfessionalsCourse ID: OSHA-13 |
![]() |
OSHA: Laser SafetyCourse ID: OSHA-14 |
![]() |
OSHA: Latex AllergyCourse ID: OSHA-15 |
![]() |
OSHA: Lockout/Tagout Control of Hazardous EnergyCourse ID: OSHA-16 |
![]() |
OSHA: Patient Abuse & NeglectCourse ID: OSHA-17 |
![]() |
OSHA: Patient RightsCourse ID: OSHA-18 |
![]() |
OSHA: Personal Protective Equipment for Healthcare WorkersCourse ID: OSHA-19 |
![]() |
OSHA: Preventing Needlestick InjuriesCourse ID: OSHA-20 |
![]() |
OSHA: Preventing Workplace Violence in Healthcare SettingsCourse ID: OSHA-21 |
![]() |
OSHA: Radiation SafetyCourse ID: OSHA-22 |
![]() |
OSHA: Safe Patient HandlingCourse ID: OSHA-23 |
![]() |
OSHA: TB Protection for Healthcare WorkersCourse ID: OSHA-24 |
![]() |
OSHA: Active Shooter ResponseCourse ID: OSHA-25 |
![]() |
OSHA: Back Care/ErgonomicsCourse ID: OSHA-26 |
![]() |
OSHA: Laboratory SafetyCourse ID: OSHA-27 |
![]() |
OSHA: Slips, Trips & FallsCourse ID: OSHA-28 |
![]() |
OSHA: Violence in the WorkplaceCourse ID: OSHA-29 |
![]() |
HR/EEO: Preventing Harassment and Discrimination for EmployeesCourse ID: HR-01 |
![]() |
HR/EEO: Preventing Harassment and Discrimination for ManagersCourse ID: HR-02 |
![]() |
HR/EEO: Preventing Sexual Harassment for EmployeesCourse ID: HR-03 |
![]() |
HR/EEO: Preventing Sexual Harassment for ManagersCourse ID: HR-04 |
Pharmaceutical Regulatory Affairs
|
|
![]() |
Global Pharmaceutical Regulatory Affairs Professional Certification ProgramCourse ID: PRA00A1 |
![]() |
US Pharmaceutical Regulatory Affairs Professional Certification ProgramCourse ID: PRA00B1 |
![]() |
Regulatory Affairs: Essentials for Human Medicinal Products – EU and USCourse ID: PRA01 |
![]() |
Regulatory Affairs: Orphan Drug Application – EU and USCourse ID: PRA02 |
![]() |
Regulatory Affairs: Preparing Submissions in the Common Technical Document (CTD) FormatCourse ID: PRA03 |
![]() |
Regulatory Affairs: Electronic Common Technical Document (eCTD)Course ID: PRA04 |
![]() |
Regulatory Affairs: Registration of Drugs Based on Monoclonal AntibodiesCourse ID: PRA05 |
![]() |
Regulatory Affairs: How to Gain Approval to Market Generic Drugs in the USACourse ID: PRA06 |
![]() |
Regulatory Affairs: Submitting a New Drug Application (NDA) to Obtain Approval to Market in the USACourse ID: PRA07 |
![]() |
Regulatory Affairs: The Regulatory Pathway to Licensing Follow-on Biologics (Biosimilars) in the USACourse ID: PRA08 |
![]() |
Regulatory Affairs: The European Centralized Procedure (CP)Course ID: PRA20 |
![]() |
Regulatory Affairs: The Mutual Recognition Procedure (MRP)Course ID: PRA21 |
![]() |
Regulatory Affairs: Variations to Marketing Authorizations in EuropeCourse ID: PRA22 |
![]() |
Regulatory Affairs: The Decentralized Procedure (DCP)Course ID: PRA23 |
![]() |
Regulatory Affairs: Essentials of Monoclonal AntibodiesCourse ID: PRA24 |
![]() |
Regulatory Affairs: The Biologics License Application (BLA) for Marketing Approval in the USACourse ID: SUB15 |
![]() |
Regulatory Affairs: The 505(b)(2) Application for Marketing Approval in the USACourse ID: SUB16 |
Pharmaceutical Sales and Marketing
|
|
![]() |
Pharmaceutical Sales & Marketing Compliance Professional CertificationCourse ID: SAMPRO |
![]() |
Pharmaceutical Sales & Marketing: Legal and Regulatory Framework for Advertising and Promotion of Prescription Drugs in the USACourse ID: SAM01 |
![]() |
Pharmaceutical Sales & Marketing: Regulatory Requirements and Guidance on Advertising and Promotion of Prescription Drugs in the USACourse ID: SAM02 |
![]() |
Pharmaceutical Sales & Marketing: Consumer-directed Advertising and Online Promotion of Prescription Drugs in the USACourse ID: SAM03 |
![]() |
Pharmaceutical Sales & Marketing: Marketing of Prescription Drugs in the USA- Interactions with Healthcare ProfessionalsCourse ID: SAM04 |
Validation for BioPharma Companies
|
|
![]() |
Pharmaceutical Validation Management Professional Certification ProgramCourse ID: VAL00S1 |
![]() |
Validation: Introduction to ValidationCourse ID: VAL01 |
![]() |
Validation: Plans and DocumentationCourse ID: VAL02 |
![]() |
Validation: Commissioning and Installation Qualification (IQ)Course ID: VAL03 |
![]() |
Validation: Operational and Performance Qualification (OQ/PQ)Course ID: VAL04 |
![]() |
Validation: Equipment Cleaning ValidationCourse ID: VAL08 |

























































































































































































