CRED Project Management for Regulatory Affairs Professionals

CRED Project Management for Regulatory Affairs Professionals
A two-day, skills-based course on the theory and practice of managing project teams to produce optimal regulatory documents and communications for those working in the pharmaceutical industry.

When
: 6-7 May 2025
Where: Online
Start time day 1: 
09:30 BST (CEST+1) | End time day 2: 17:15 BST (CEST+1)

This course is also available to attend in person.

Suitable for

This course is designed for those:

  • Regulatory staff at establishing to driving level working in any aspect of regulatory affairs where they are involved in delivering or managing projects
  • For more senior staff who are running complex projects or managing a range of projects and want to make sure they have up to date skills and gain from shared expertise
  • Project Managers with responsibility for regulatory projects who want to understand regulatory aspects

Course information

During this course you will:

  • Learn how to scope and deliver complex regulatory projects to tight timelines
  • Get insights into how to effectively manage documentation
  • Understand how to assess and manage risks to the project
  • Gain skills to work effectively with teams and stakeholders



Benefits to delegates

  • Meet and learn from experts in the field   
  • Learn by doing - participate in case studies and interactive sessions 
  • Build a network to support the rest of your career 
  • Acquire a toolkit to help you deliver projects on time and to the required standard more easily
  • Enhance your reputation as an effective project manager
  • Become more confident at managing projects and the associated workload
  • Reduce your stress levels by learning how to manage difficult people on your project teams
  • Increase engagement in your project teams
  • Manage your workload by gaining tips for effective delegation
  • Take a course designed by professionals for professionals with a proven track record 
CPD: This course provides 14 CPD hours upon successful completion

To learn more about why Continuing Professional Development is important, visit our Lifelong Learning page.

Programme

Download a copy of the programme here.

 

Presenters 

  • Gurdeep Bhangra, Associate Director, IQVIA, MTOPRA
  • Joe Cheal, Lead Imaginarian, Imaginarium Learning & Development
  • Oliver Rick, Regulatory Affairs Programme Manager, Independent Consultant, MTOPRA
  • Sinéad Usher, Regulatory Affairs Consultant & Director, SMART Regulatory Services Ltd, MTOPRA

Pricing

 Standard training course registration fees
 Event Registration Type Price (GBP)
 Standard Price 
 TOPRA Member
£1,050.00 + VAT*
 Standard Price
 Non-member
£1,250.00 + VAT* 

Save on the full cost of membership and £180
on the price of your training
course when you add TOPRA membership to your booking (membership fees are exempt from VAT).
*VAT, where applicable, is charged at the rate of 20%.
 
 Discounted training course registration fees
 Event Registration Type Price (GBP)
 Government or academic rates
 TOPRA Member
£787.50 + VAT*
 Government or academic rates 
 Non-member
£937.50 + VAT*
 Charities, patient groups, full-time education rates
 
TOPRA Member
£525.00 + VAT*
  Charities, patient groups, full-time education rates
  Non-member
 £625.00 + VAT*

Places are also available for those in low-income countries as defined by the World Bank.
*VAT, where applicable, is charged at the rate of 20%.

Terms and conditions

By booking a place on this course you are agreeing to the training terms and conditions.

When
06/05/2025 - 07/05/2025
Where
ONLINE
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