2024 Trends in Clinical Trial Design |
Intermediate |
Clinical Trial Methodology |
Benefit-risk assessment and pharmacovigilance |
Beginner |
Clinical Trial Management |
Certificado de Investigador Clínico |
3 levels of progress |
GCP |
Clinical Trial Design |
Intermediate |
Clinical Trial Methodology |
Clinical trial design - basics of statistical analysis |
Advanced |
Clinical Trial Methodology |
Clinical Trials Information System (CTIS) |
Beginner |
Clinical Trial Management |
Clinical Trials Operations Specialization |
Beginner |
Clinical Trial Management |
Community Advisory Boards |
Intermediate |
Patients Engagement |
CONSCIOUS I Curriculum Chapter 10: The numbers…sample size, why it’s important; Interpreting the Results |
Beginner |
Clinical Trial Methodology |
CONSCIOUS I Curriculum Chapter 11: Medical Devices and Advance Therapies |
Beginner |
Clinical Trial Methodology CT Regulations/Ethics |
CONSCIOUS I Curriculum Chapter 13: Adverse events and reporting responsibilities |
Beginner |
Clinical Trial Management |
CONSCIOUS I Curriculum Chapter 4: Ethics in Clinical Trials |
Beginner |
CT Regulations/Ethics |
CONSCIOUS I Curriculum Chapter 5: What patients should know _ informed consent |
Beginner |
Clinical Trial Management |
CONSCIOUS I Curriculum Chapter 6: Equipoise; Forming a research question and defining the outcome |
Beginner |
Clinical Trial Methodology |
CONSCIOUS I Curriculum Chapter 8: Phase 3 trial design |
Beginner |
Clinical Trial Methodology |
CONSCIOUS I Curriculum Chapter 9: The clinical trial protocol & case report forms (CRF) |
Beginner |
Clinical Trial Management |
CONSCIOUS I Curriculum Chapter7: Clinical Trial Phases |
Beginner |
Clinical Trial Methodology |
CONSCIOUS II Curriculum Chapter 1 - Clinical Trial Design |
Intermediate |
Clinical Trial Methodology |
CONSCIOUS II Curriculum Chapter 10 - Leadership for 21st Century Trialists |
Intermediate |
Clinical Trial Management |
CONSCIOUS II Curriculum Chapter 2 - Trial Methodology |
Intermediate |
Clinical Trial Methodology |
CONSCIOUS II Curriculum Chapter 3 - Trial Management |
Intermediate |
Clinical Trial Management |
CONSCIOUS II Curriculum Chapter 4 - Quality and Regulatory Affairs |
Intermediate |
Clinical Trial Management CT Regulations/Ethics |
CONSCIOUS II Curriculum Chapter 5 - Pharmacovigilance and Study Medication |
Intermediate |
Clinical Trial Management |
CONSCIOUS II Curriculum Chapter 6 - Data Management and Statistical Analysis |
Intermediate |
Clinical Trial Management |
CONSCIOUS II Curriculum Chapter 7 - Early Phase Trials |
Intermediate |
Clinical Trial Methodology |
CONSCIOUS II Curriculum Chapter 8 - Paediatric Clinical Trials |
Intermediate |
Clinical Trial Methodology CT Regulations/Ethics |
CONSCIOUS II Curriculum Chapter 9 - Medical Devices |
Intermediate |
Clinical Trial Methodology |
CTMC 2021 Webinar Series: Adverse Event and Safety Reporting |
Intermediate |
Clinical Trial Management |
CTMC 2021 Webinar Series: Pearls and Pitfalls when considering an early phase clinical trial |
Intermediate |
Clinical Trial Methodology |
CTMC 2021 Webinar Series: Pilot and Feasibility Trials |
Intermediate |
Clinical Trial Methodology |
CTMC 2021 Webinar Series: Trial Management |
Beginner |
Clinical Trial Management |
CTMC 2021 Webinar Series: What to Know About Sample Size |
Intermediate |
Clinical Trial Methodology |
Data Management for Clinical Research |
Beginner |
Clinical Trial Management |
Design and Interpretation of Clinical Trials |
Beginner |
Clinical Trial Methodology |
Ethics |
Beginner |
CT Regulations/Ethics |
Ethics in clinical trials |
Beginner |
CT Regulations/Ethics |
Ethics in science? |
Beginner |
CT Regulations/Ethics |
EUPATI Ethics Committee |
Beginner |
CT Regulations/Ethics |
Formations "Bonnes Pratiques Des Essais Cliniques" |
2 levels: Investigator and Sponsor |
GCP |
Fundamentals of statistics in clinical trials |
Beginner |
Clinical Trial Methodology |
Good Clinical Practice |
Beginner |
GCP |
Good Clinical Practice (GCP) Refresher ELearning |
Advanced |
GCP |
Good Clinical Practice - ICH Guidelines E6 R2 |
Beginner |
GCP |
Grant Writing for Non-Profits |
Beginner |
Proposal Writing |
ICH Good Clinical Practice E6 (R2) |
Beginner |
GCP |
ICH-GCP : Good Clinical Practice |
Beginner |
GCP |
International Program for site staff conducting clinical research |
Beginner |
Clinical Trial Management |
Introduction to Clinical Trials: The Basics |
Beginner |
Clinical Trial Methodology |
Introduction to the Clinical Trials Regulation |
Beginner |
CT Regulations/Ethics |
Introduction to the Principles and Practice of Clinical Research (IPPCR) |
Beginner |
Clinical Trial Management |
Kurs i Good Clinical Practice 2 (GCP2) |
Beginner |
GCP |
Master Your Clinical Trial Budget:A Step-by-Step Guide to Smart Clinical Expense Planning |
Intermediate |
Clinical Trial Management |
Medical Regulatory Framework and Procedures |
Beginner |
CT Regulations/Ethics |
Medical Research and Development |
Beginner |
Clinical Trial Methodology |
Patient Engagement |
Intermediate |
Patients Engagement |
Patient Engagement Resources |
Beginner/Intermediate |
Patients Engagement |
Process of Medicines Discovery and Development |
Beginner |
Clinical Trial Methodology |
Proposal Writing Training for Collaborative Projects in Horizon Europe |
Beginner |
Proposal Writing |
Safety in Clinical Trials |
Beginner |
Clinical Trial Management |
Safety Management in Clinical Research. Medical Devices |
Beginner |
Clinical Trial Management |
Site Management Modules |
Beginner |
Clinical Trial Management |
The European Medicines Agency (EMA) |
Beginner |
CT Regulations/Ethics |
The impact of GDPR on clinical trials |
Beginner |
CT Regulations/Ethics |
Training and Resources in Research Ethics Evaluation (TRREE) |
Beginner |
CT Regulations/Ethics |
Training on Horizon Europe proposal writing - Part 1 of 2 |
Beginner |
Proposal Writing |
Training on Horizon Europe proposal writing - Part 2 of 2 |
Beginner |
Proposal Writing |
Webinar on the Annotated Horizon Europe Template "Information on Clinical Studies" |
Beginner |
Proposal Writing |