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Accredited compliance and regulatory trainings designed for life sciences

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GDP : Good Distribution Practices

Good Distribution Practice

GMP : Good Manufacturing Practices

Introduction To Good Manufacturing Practice (GMP)

GLP : Good Laboratory Practices

Introduction to Good Laboratory Practice (GLP)

GMP : Good Manufacturing Practices

Good Documentation Practice (GDocP)

GCP : Clinical Trials

ICH-GCP: Introduction to Good Clinical Practice

GMP : Good Manufacturing Practices

Corrective Action and Preventive Action (CAPA) Training

GCP : Clinical Trials

ICH-GCP Training Refresher 2023 : Good Clinical Practice for Clinical Research Professionals

GDP : Good Distribution Practices

Introduction to FDA 21 CFR PART 11 Online Course

GMP : Good Manufacturing Practices

GMP Documentation and Record Retention

GDP : Good Distribution Practices

Introduction to Current Good Practice (CGXP)

GCP : Clinical Trials

GMP for clinical trials manufacture and supply

GMP : Good Manufacturing Practices

An Introduction to Good Manufacturing Practices in the EU

GLP : Good Laboratory Practices

Regulatory Compliance Inspections and External Audits

Quality Assurance

Pharmaceutical Data Integrity : ALCOA and ALCOA+

Clinical Data Management

GCP : Clinical Trials

Clinical Data Management

GMP : Good Manufacturing Practices

Overview of Qualification and Validation

Pharmacovigilance

Introduction to GxP

Pharmacovigilance

Global Pharmacovigilance Awareness

Regulatory Affairs

Pharmaceutical Regulatory Affairs

Quality Assurance

Records, Archiving, and Retention

GMP : Good Manufacturing Practices

Management of Service Providers

GMP : Good Manufacturing Practices

Quality Management for Medical Devices – ISO 13485:2016

GCP : Clinical Trials

Pharmacovigilance Case Handling

GMP : Good Manufacturing Practices

Quality Risk Management

Quality Assurance

Introduction to Pharmaceutical Quality

Pharmacovigilance

Introduction to Good Pharmacovigilance Practice (GVP)

GMP : Good Manufacturing Practices

GMP for Food Safety and ISO 22000

GCP : Clinical Trials

Management of Periodic Safety Update Reports

GCP : Clinical Trials

Management of The TMF and ISF

Pharmacovigilance

Screening and Management of Literature for Pharmacovigilance Activities

GMP : Good Manufacturing Practices

GMP for Medical Devices and FDA 21 CFR PART 820

Pharmacovigilance

Management of Drug Safety Concern Through a Pharmacovigilance Steering Committee

GCP : Clinical Trials

Management of Clinical Study Reports

GMP : Good Manufacturing Practices

Computer System Validation (CSV)

GCP : Clinical Trials

Introduction to Clinical Trial Protocols

GCP : Clinical Trials

Clinical Trials : Preparing for an audit or an inspection

GMP : Good Manufacturing Practices

GMP for Medical Devices: EU versus FDA

Pharmacovigilance

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

GCP : Clinical Trials

Selection of Trial Sites

GCP : Clinical Trials

Non-Interventional Studies (NIS) Module 2: Practical Aspect

Regulatory Affairs

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

Quality Assurance

Risk Analysis Model for Management of Quality Risk

GCP : Clinical Trials

Randomization Process and Unblinding for Analysis

GCP : Clinical Trials

Non-Interventional Studies (NIS) Module 1: General Principles

GCP : Clinical Trials

Investigational Medicinal Product Order for Clinical Studies

Quality Assurance

Statistical Process Control

GDP : Good Distribution Practices

Pharmaceutical Warehouses Practices

GCP : Clinical Trials

Registration of Trials on clinicaltrials.gov

GCP : Clinical Trials

Management of Externally Sponsored Studies

GCP : Clinical Trials

Clinical Management of Non-Interventional Studies

GCP : Clinical Trials

Human Biological Samples Handling

GCP : Clinical Trials

First in Human Safety Assessment (FIHSA) Dossier