GDP/GxP foundations
Core regulatory understanding and practical application for operational teams, quality teams and leaders.
Training
Expert-led pharmaceutical quality learning for the responsibilities, risks and real decisions your people face every day.

Designed to be used
Our programmes support GDP, GxP, Good Clinical Practice (GCP), quality systems, Responsible Person responsibilities, data integrity, deviations, CAPA and documentation standards.
Rather than relying on generic theory, Setax uses practical examples, role-relevant discussion and clear next steps to help learning transfer into everyday practice.
Discuss training needsLearning areas
Core regulatory understanding and practical application for operational teams, quality teams and leaders.
Practical GCP training for clinical research teams, covering participant safety, data integrity, essential documentation, roles, responsibilities and inspection readiness.
Targeted learning for RP and RPi responsibilities, oversight, accountability and decision-making.
Improve SOP, deviation, CAPA, audit and data-integrity documentation with stronger consistency.
Prepare teams to explain their processes, evidence effective practice and respond with confidence.
Guidance on responsible use of AI tools within controlled pharmaceutical quality workflows.
Training shaped around your roles, current risks, processes and intended quality outcomes.
A clear sequence
We identify your people, learning needs, risks and desired outcomes.
We tailor content around roles, processes and the situations your teams face.
Expert-led learning brings regulations to life through practical discussion.
Evaluation and follow-up support help turn learning into sustained practice.
The outcome
Well-designed training supports standardised procedures, greater inspection readiness, a stronger QMS and preventative ways of working.
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