Online Certified Courses designed for Pharmaceuticals

GMP : Good Manufacturing Practices

Introduction To Good Manufacturing Practice (GMP)

Food and Nutrition

Good Distribution Practice

Contract Research Organization (CRO)

Good Documentation Practice (GDocP)

Food and Nutrition

Introduction to Good Laboratory Practice (GLP)

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

GMP : Good Manufacturing Practices

Introduction to Pharmaceutical Quality

Contract Research Organization (CRO)

Introduction to Good Pharmacovigilance Practice (GVP)

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

Cross-Industry

Quality Risk Management

GMP : Good Manufacturing Practices

CFRs Part 210 and 211 : cGMPs for Finished Pharmaceuticals

Contract Research Organization (CRO)

How to write effective Standard Operating Procedures (SOPs)

Cross-Industry

Introduction to Current Good Practice (CGXP)

GMP : Good Manufacturing Practices

Internal GMP Audit & Role of GMP Auditor

Pharmaceuticals

Pharmacovigilance Case Handling

GMP : Good Manufacturing Practices

An Introduction to Good Manufacturing Practices in the EU

Contract Research Organization (CRO)

Introduction to Software Validation Assurance

Contract Research Organization (CRO)

21 CFR Part 58: GLP for Nonclinical Laboratories

GMP : Good Manufacturing Practices

Cleaning Validation Course

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

GMP : Good Manufacturing Practices

GMP Refresher 2025

Contract Research Organization (CRO)

Management of Clinical Study Reports

GDP : Good Distribution Practices

Pharmaceutical Warehouses / Storage Practices

GMP : Good Manufacturing Practices

GMP Documentation and Record Retention

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

Medical Devices

Management of Drug Safety Concern Through a Pharmacovigilance Steering Committee

Contract Research Organization (CRO)

Management of Service Providers

GMP : Good Manufacturing Practices

GMP for Pharmaceutical Packaging and ISO 15378

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)

Human Biological Samples Handling

GMP : Good Manufacturing Practices

CMC: Chemistry, Manufacturing, and Controls

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)

Medical Devices

Risk Analysis Model for Management of Quality Risk

Pharmaceuticals

ISO 9001:2015 : Quality Management System for Pharmaceuticals

Contract Research Organization (CRO)

Randomization & Blinding in Clinical Research Trials

Hospitals & Healthcare Institutions

Signal Detection and Management in Pharmacovigilance

Contract Research Organization (CRO)

Investigational Medicinal Product Order for Clinical Studies

Contract Research Organization (CRO)

21 CFR PART 50 Informed Consent of Human Subjects

Pharmaceuticals

PIC/S Compliance: A Comprehensive Guide for Pharmaceutical and Hospital Professionals

Contract Research Organization (CRO)

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

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

Pharmaceuticals

Submitting a New Drug Application (NDA) in the USA