This course provides a comprehensive and structured overview of Project Management methodologies applied to the pharmaceutical and medical device sectors. It integrates regulatory frameworks, quality systems, validation processes, and Agile methods adapted to GxP environments. Through lectures, case analyses, practical exercises, and applied project work, learners gain skills in initiating, planning, executing, monitoring, and closing projects within regulated contexts

Aims

- Provide a strong foundational understanding of Project Management in regulated pharmaceutical environments.
- Develop the ability to initiate, plan, execute, monitor, and close projects aligned with compliance and quality requirements.
- Strengthen learners’ capability to integrate regulatory frameworks into project planning and execution.
- Enhance team management, communication, and leadership skills in cross-functional project settings.
- Enable practical application of Agile and traditional PM methodologies within GxP constraints.
- Cultivate problem-solving and decision-making abilities in complex regulated project scenarios.

Hosted by
  • SUPSI
Event date
Event starts in
  • 60

    Days
  • 04

    Hours
  • 14

    Minutes
Location