CAPA en industrie pharma : bonnes pratiques, erreurs à éviter (avec Qualnet)

In this video, we break down the CAPA process in the pharmaceutical industry: corrective actions, preventive actions, GMP requirements, common errors, and best practices for a truly effective quality system. To discover our partner Qualnet and their digital solutions: https://www.qualnet.fr With Rémy and Yann from Qualnet, we discuss the difference between CAPA, corrective action, investigation, deviation, and change control, as well as digitalization, workflow, effectiveness review, delays, responsibilities, and quality management. The goal: to eliminate unnecessary, poorly defined, or "just for show" CAPAs and get back to basics: SMART actions—relevant, measurable, and truly useful for continuous improvement. On the agenda: Corrective vs. preventive CAPA, common pitfalls, the link with deviations and complaints, GMP expectations, closure criteria, effectiveness measurement, delays, and practical advice for strengthening the quality maturity of a pharmaceutical site. Join this channel to get access to exclusive benefits:    / @qppharma4182