Regulatory Environment Impact on Project Management in the Pharmaceutical Industry

Description

This 1-day seminar is intended to help participants understand how regulatory activities are inherent to most pharma projects and must be anticipated by pharmaceutical project managers.

This seminar will enable participants to better understand the impact of regulatory activities on their projects in order to improve planning and delivery performance.

Learning Objectives

After this seminar, you will be able to:

1. keep up to date on the latest updates to project management guidelines (predictive, hybrid, adaptive) to deal with the impact of the regulatory environment on project baselines (scope, schedule, cost)
2. provide a fundamental understanding of the various key principles of regulation in the pharmaceutical environment and associated terminology
3. support the smooth running of projects by identifying the main regulatory steps that may impact project planning activities
4. practice in small groups to solve regulatory constraints and deliver a project as early as possible

Delivery Methods

• ✅ Live in-person (classroom)

PDU Allocation

TOTAL PDUs = 8

• Ways of Working: 2
• Power Skills: 3
• Business Acumen: 3

Languages

• English