| Greetings!
Every drug begins with trust. A patient swallows a tablet believing it will heal, not harm. Behind that moment lies a silent promise that can break the instant a process drifts from Good Manufacturing Practice.
This workshop examines that fragile space between compliance and collapse. It explores the purpose and history of GMP, the systems that uphold it, and the decisions that quietly erode it. Participants will study not only what GMP requires but why it exists: to protect the patient, preserve the science, and sustain the credibility of every label on a bottle.
The session walks through the full chain of compliance from documentation and validation to change control, sanitation, and audit readiness. Case discussions reveal the mechanics of deviation management, production controls, and inspection strategy.
Whether you lead, supervise, or support manufacturing and quality operations, this session restores clarity to what is often dismissed as routine paperwork. GMP is not bureaucracy. It is the architecture of trust that holds the pharmaceutical industry together. By the end of this half-day program, participants gain a working command of GMP implementation, documentation accuracy, and audit preparedness through real examples that connect regulation with consequence. | 
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