Portfolio

All Storyline Rise Video

Document Control System

Learn the essentials of GMP document control—how documents are created, maintained, and archived to ensure data integrity and compliance. This module provides quick, practical guidance for stronger quality and audit readiness.

Issue Management - The Process

E-Learning | Storyline

This module provides a clear, structured overview of how to manage quality issues in a GMP environment—explaining the who, when, why, and how behind a systematic and efficient issue-handling process.

Introduction to risk

E-Learning | Storyline

This Articulate Storyline module provides a clear, engaging overview of core risk management—covering types of risks, key processes, control strategies, and the vital role of management in effective risk oversight.

Types of Documentation

E-Learning | Rice

This module offers a clear introduction to GMP documentation—explaining the difference between documents and records, key documents used in Production and Quality Control, and the purpose of a Site Master File.

Serious adverse events

E-Learning | Rice

This module covers how to identify, assess, and report Serious Adverse Events (SAEs), outlining key criteria such as hospitalisation, death, life-threatening conditions, disability, and other medically important events.

Introduction to Deviations Process

E-Learning | Rice

This module delivers a clear, streamlined overview of deviation management—covering when to record, how to investigate, and how to close deviations, along with key roles, responsibilities, and the importance of meeting strict GMP timelines.

Six - thinking hat

Video

This eLearning video simplifies Edward de Bono’s Six Thinking Hats, showing how structured perspectives boost clarity, creativity, and decision-making in meetings through a clear, practical example.

Deviations process - pract

Video

This eLearning video delivers a clear, well-designed overview of deviation management in pharma—explaining what deviations are, why they matter, and the key steps to identify, investigate, and close them for stronger GMP compliance.