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GCP : Clinical Trials

ICH-GCP: Introduction to Good Clinical Practice

GDP : Good Distribution Practices

Introduction to FDA 21 CFR PART 11 Online Course

Pharmacovigilance

Introduction to GxP

GCP : Clinical Trials

Regulatory Compliance Inspections and External Audits

Regulatory Affairs

Pharmaceutical Regulatory Affairs

GCP : Clinical Trials

GMP for clinical trials manufacture and supply

GDP : Good Distribution Practices

Introduction to Current Good Practice (CGXP)

Quality Assurance

How to write effective Standard Operating Procedures (SOPs)

GMP : Good Manufacturing Practices

An Introduction to Good Manufacturing Practices in the EU

Clinical Data Management

Clinical Data Management

GCP : Clinical Trials

Clinical Data Management

Medical Devices

ISO 14971: Risk Management For Medical Devices

GMP : Good Manufacturing Practices

Internal GMP Audit & Role of GMP Auditor

Pharmacovigilance

Screening and Management of Literature for Pharmacovigilance Activities

Medical Devices

Medical Device Regulation – MDR 2017/745

GMP : Good Manufacturing Practices

GMP Refresher 2025

GMP : Good Manufacturing Practices

IVDR Training : In Vitro Diagnostic Medical Devices Regulation 2017/746

GCP : Clinical Trials

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

Medical Devices

GMP for Medical Devices: EU versus FDA

Quality Assurance

Statistical Process Control

GCP : Clinical Trials

21 CFR PART 50 Informed Consent of Human Subjects

GCP : Clinical Trials

Randomization & Blinding in Clinical Research Trials

Regulatory Affairs

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