Online Certified Courses for CROs

Certified online training for CRO professionals collaborating with sponsors and pharma companies. Gain expertise in GCP, pharmacovigilance, and clinical trials regulations. 100% Audit-ready !

+3.000 organizations and individuals have been certified

Courses

X

Contract Research Organization (CRO)

Good Documentation Practice (GDocP)

Contract Research Organization (CRO)

ICH-GCP: Introduction to Good Clinical Practice

Contract Research Organization (CRO)

Introduction to FDA 21 CFR PART 11 Online Course

Contract Research Organization (CRO)

Pharmaceutical Data Integrity : ALCOA and ALCOA+

Contract Research Organization (CRO)

Computer System Validation (CSV) and GAMP 5

Contract Research Organization (CRO)

Corrective Action and Preventive Action (CAPA) Training

Contract Research Organization (CRO)

Introduction to Good Pharmacovigilance Practice (GVP)

Contract Research Organization (CRO)

Good Clinical Laboratory Practice (‎GCLP)‎

Contract Research Organization (CRO)

Introduction to GxP

Contract Research Organization (CRO)

Pharmaceutical Regulatory Affairs

Contract Research Organization (CRO)

Regulatory Compliance Inspections and External Audits

Contract Research Organization (CRO)

GMP for clinical trials manufacture and supply

Contract Research Organization (CRO)

How to write effective Standard Operating Procedures (SOPs)

Contract Research Organization (CRO)

Introduction to Software Validation Assurance

Contract Research Organization (CRO)

21 CFR Part 58: GLP for Nonclinical Laboratories

Contract Research Organization (CRO)

Management of The TMF and ISF

Contract Research Organization (CRO)

Global Pharmacovigilance Awareness

Contract Research Organization (CRO)

Screening and Management of Literature for Pharmacovigilance Activities

Contract Research Organization (CRO)

Management of Clinical Study Reports

Contract Research Organization (CRO)

General Data Protection Regulation (GDPR) for Pharmaceuticals and Clinical Trials

Contract Research Organization (CRO)

Management of Periodic Safety Update Reports (PSURs)

Contract Research Organization (CRO)

Clinical Management of Non-Interventional Studies

Contract Research Organization (CRO)

Records, Archiving, and Retention

Contract Research Organization (CRO)

First in Human Safety Assessment (FIHSA) Dossier

Contract Research Organization (CRO)

Management of Service Providers

Contract Research Organization (CRO)

OSHA Lab Safety Certified Training

Contract Research Organization (CRO)

Human Biological Samples Handling

Contract Research Organization (CRO)

Anti-Bribery and Anti-Corruption Certified Training Course : ISO37001

Contract Research Organization (CRO)

Clinical Trials : Preparing for an audit or an inspection

Contract Research Organization (CRO)

Selection of Trial Sites

Contract Research Organization (CRO)

Medical Writing of Periodic Benefit-Risk Evaluation Report (PBRER)

Contract Research Organization (CRO)

Introduction to Non-Interventional Studies (NIS)

Contract Research Organization (CRO)

Randomization & Blinding in Clinical Research Trials

Contract Research Organization (CRO)

Investigational Medicinal Product Order for Clinical Studies

Contract Research Organization (CRO)

21 CFR PART 50 Informed Consent of Human Subjects

Contract Research Organization (CRO)

Registration of Trials on clinicaltrials.gov

Contract Research Organization (CRO)

Management of Externally Sponsored Studies

Contract Research Organization (CRO)

Cybersecurity in Life Sciences and Healthcare

Contract Research Organization (CRO)

Procedure for Handling Cases of Suspected Serious Breach, Misconduct & Fraud