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Accredited compliance and regulatory trainings designed for life sciences



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General Data Protection Regulation (GDPR) for Pharmaceuticals and Clinical Trials
(Category : GCP : Clinical Trials / GLP : Good Laboratory Practices)
(Category : GCP : Clinical Trials / GLP : Good Laboratory Practices)
GMP for Pharmaceutical Packaging and ISO 15378
(Category : GMP : Good Manufacturing Practices / Quality Assurance)
(Category : GMP : Good Manufacturing Practices / Quality Assurance)
IVDR Training : In Vitro Diagnostic Medical Devices Regulation 2017/746
(Category : GMP : Good Manufacturing Practices / Medical Devices / Regulatory Affairs)
(Category : GMP : Good Manufacturing Practices / Medical Devices / Regulatory Affairs)
Laboratory Management Systems – ISO/IEC 17025:2017
(Category : GCP : Clinical Trials / GLP : Good Laboratory Practices)
(Category : GCP : Clinical Trials / GLP : Good Laboratory Practices)
21 CFR Part 58: GLP for Nonclinical Laboratories
(Category : GCP : Clinical Trials / GLP : Good Laboratory Practices)
(Category : GCP : Clinical Trials / GLP : Good Laboratory Practices)
Good Clinical Laboratory Practice (GCLP)
(Category : GCP : Clinical Trials / GLP : Good Laboratory Practices)
(Category : GCP : Clinical Trials / GLP : Good Laboratory Practices)
ISO 14971: Risk Management For Medical Devices
(Category : Medical Devices / Quality Assurance / Regulatory Affairs)
(Category : Medical Devices / Quality Assurance / Regulatory Affairs)
How to write effective Standard Operating Procedures (SOPs)
(Category : Quality Assurance / Regulatory Affairs)
(Category : Quality Assurance / Regulatory Affairs)
Anti-Bribery and Anti-Corruption Certified Training Course : ISO37001
(Category : GCP : Clinical Trials / GDP : Good Distribution Practices / GLP : Good Laboratory Practices / GMP : Good Manufacturing Practices / Pharmacovigilance / Quality Assurance / Regulatory Affairs)
(Category : GCP : Clinical Trials / GDP : Good Distribution Practices / GLP : Good Laboratory Practices / GMP : Good Manufacturing Practices / Pharmacovigilance / Quality Assurance / Regulatory Affairs)
Cleaning Validation Course
(Category : GLP : Good Laboratory Practices / GMP : Good Manufacturing Practices)
(Category : GLP : Good Laboratory Practices / GMP : Good Manufacturing Practices)
CFRs Part 210 and 211 : cGMPs for Finished Pharmaceuticals
(Category : GMP : Good Manufacturing Practices)
(Category : GMP : Good Manufacturing Practices)
HACCP : Hazard Analysis and Critical Control Point System
(Category : GMP : Good Manufacturing Practices / Quality Assurance)
(Category : GMP : Good Manufacturing Practices / Quality Assurance)
Internal GMP Audit & Role of GMP Auditor
(Category : GMP : Good Manufacturing Practices / Regulatory Affairs)
(Category : GMP : Good Manufacturing Practices / Regulatory Affairs)
21 CFR PART 50 Informed Consent of Human Subjects
(Category : GCP : Clinical Trials / Regulatory Affairs)
(Category : GCP : Clinical Trials / Regulatory Affairs)
Medical Device Regulation - MDR 2017/745
(Category : Medical Devices / Quality Assurance / Regulatory Affairs)
(Category : Medical Devices / Quality Assurance / Regulatory Affairs)
Pharmaceutical Warehouses / Storage Practices
(Category : GDP : Good Distribution Practices / GMP : Good Manufacturing Practices)
(Category : GDP : Good Distribution Practices / GMP : Good Manufacturing Practices)
Medical Writing of Periodic Benefit-Risk Evaluation Report (PBRER)
(Category : Pharmacovigilance / Quality Assurance)
(Category : Pharmacovigilance / Quality Assurance)
Randomization & Blinding in Clinical Research Trials
(Category : GCP : Clinical Trials / Regulatory Affairs)
(Category : GCP : Clinical Trials / Regulatory Affairs)
ICH-GCP Training Refresher 2025 : Good Clinical Practice for Clinical Research Professionals
(Category : GCP : Clinical Trials)
(Category : GCP : Clinical Trials)
GMP for clinical trials manufacture and supply
(Category : GCP : Clinical Trials / GMP : Good Manufacturing Practices / Regulatory Affairs)
(Category : GCP : Clinical Trials / GMP : Good Manufacturing Practices / Regulatory Affairs)
Good Documentation Practice (GDocP)
(Category : GMP : Good Manufacturing Practices / Quality Assurance)
(Category : GMP : Good Manufacturing Practices / Quality Assurance)
GMP for Medical Devices and FDA 21 CFR PART 820
(Category : GMP : Good Manufacturing Practices / Medical Devices)
(Category : GMP : Good Manufacturing Practices / Medical Devices)
ICH-GCP: Introduction to Good Clinical Practice
(Category : GCP : Clinical Trials / Regulatory Affairs)
(Category : GCP : Clinical Trials / Regulatory Affairs)
Quality Management for Medical Devices - ISO 13485:2016
(Category : GMP : Good Manufacturing Practices / Medical Devices / Quality Assurance)
(Category : GMP : Good Manufacturing Practices / Medical Devices / Quality Assurance)
Introduction to FDA 21 CFR PART 11 Online Course
(Category : GDP : Good Distribution Practices / GMP : Good Manufacturing Practices / Quality Assurance / Regulatory Affairs)
(Category : GDP : Good Distribution Practices / GMP : Good Manufacturing Practices / Quality Assurance / Regulatory Affairs)
An Introduction to Good Manufacturing Practices in the EU
(Category : GMP : Good Manufacturing Practices / Quality Assurance / Regulatory Affairs)
(Category : GMP : Good Manufacturing Practices / Quality Assurance / Regulatory Affairs)
GMP Documentation and Record Retention
(Category : GMP : Good Manufacturing Practices / Quality Assurance)
(Category : GMP : Good Manufacturing Practices / Quality Assurance)
Screening and Management of Literature for Pharmacovigilance Activities
(Category : Pharmacovigilance / Quality Assurance / Regulatory Affairs)
(Category : Pharmacovigilance / Quality Assurance / Regulatory Affairs)
Human Biological Samples Handling
(Category : GCP : Clinical Trials / GDP : Good Distribution Practices)
(Category : GCP : Clinical Trials / GDP : Good Distribution Practices)
Management of Service Providers
(Category : GDP : Good Distribution Practices / GMP : Good Manufacturing Practices / Quality Assurance)
(Category : GDP : Good Distribution Practices / GMP : Good Manufacturing Practices / Quality Assurance)
Clinical Management of Non-Interventional Studies
(Category : GCP : Clinical Trials / Pharmacovigilance / Quality Assurance)
(Category : GCP : Clinical Trials / Pharmacovigilance / Quality Assurance)
Introduction to Non-Interventional Studies (NIS)
(Category : GCP : Clinical Trials / Pharmacovigilance)
(Category : GCP : Clinical Trials / Pharmacovigilance)
Procedure for Handling Cases of Suspected Serious Breach, Misconduct & Fraud
(Category : Regulatory Affairs)
(Category : Regulatory Affairs)
Management of Periodic Safety Update Reports (PSURs)
(Category : Pharmacovigilance / Quality Assurance)
(Category : Pharmacovigilance / Quality Assurance)
Management of Drug Safety Concern Through a Pharmacovigilance Steering Committee
(Category : Pharmacovigilance / Quality Assurance)
(Category : Pharmacovigilance / Quality Assurance)
Introduction to Pharmaceutical Quality
(Category : GMP : Good Manufacturing Practices / Quality Assurance)
(Category : GMP : Good Manufacturing Practices / Quality Assurance)
Overview of Qualification and Validation
(Category : GMP : Good Manufacturing Practices / Quality Assurance)
(Category : GMP : Good Manufacturing Practices / Quality Assurance)
Introduction to Current Good Practice (CGXP)
(Category : GDP : Good Distribution Practices / GLP : Good Laboratory Practices / Quality Assurance / Regulatory Affairs)
(Category : GDP : Good Distribution Practices / GLP : Good Laboratory Practices / Quality Assurance / Regulatory Affairs)
Regulatory Compliance Inspections and External Audits
(Category : GCP : Clinical Trials / GMP : Good Manufacturing Practices / Medical Devices / Regulatory Affairs)
(Category : GCP : Clinical Trials / GMP : Good Manufacturing Practices / Medical Devices / Regulatory Affairs)
Corrective Action and Preventive Action (CAPA) Training
(Category : GMP : Good Manufacturing Practices)
(Category : GMP : Good Manufacturing Practices)
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