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Good Manufacturing Practices – bases and practices  training in english / formation en français

Continuing training is included in GMP as a key element of the pharmaceutical quality system. Responding to industry needs, this GMP training course was developed and facilitated by pharmaceutical industry experts. A global presentation of GMP as well as a reminder of GMP news are on the agenda. But more than just a training, this is a unique opportunity for participants to join a network of local professionals, exchange experiences and thus participate in the dynamism of the area.

Learning objectives

Content / Topics addressed


Target group

Duration of training


Conservez et fructifiez vos acquis !

La plupart des modules de formation suivis à l’ARIAQ s’inscrivent dans un cursus professionnalisant. Vous conservez pendant 2 ans le bénéfice de votre formation initiale, puis vous complétez à votre rythme, votre parcours de formation pour atteindre la certification ultime de :

« Quality Assurance Specialist »
liste des modules concernés

« Regulatory Affairs Specialist »
liste des modules concernés

« Quality and Regulatory Specialist »
liste des modules concernés

La règlementation et les normes techniques évoluant au cours du temps, le contenu des modules d’expertises proposés dans ces cursus, peut être amené à varier. En cas de changement majeur concernant un module d’expertise déjà réalisé, il est recommandé de suivre à nouveau ce module.
Vous pouvez solliciter l’analyse de notre Expert via notre Formulaire de contact


The dates for this training are not yet fixed. Do not hesitate to reserve your place without engagement if you are interested in this training.

Good Manufacturing Practices – bases and practices

Click to reserve

CHF 750.–

Our prices include breaks, lunch and documents.
VAT not included on catering fees.


Vu Thanh Liem

Pharmacist, PhD in Pharmaceutical Sciences with more than 20 years of experience in the pharmaceutical industry in the field of quality assurance, validation and production. Currently QA Director and Qualified Person for Debiopharm Research & Manufacturing SA.

Mickael Brégand