The Regulatory Environment in the USA

The Regulatory Environment in the USA
Master the complexities of U.S. regulatory operations and gain the expertise to navigate FDA processes with confidence. This course is also Module 11 of the MSc programme.


This course is  also available to attend online.






When:
 
24 - 26 March 2026
Where: 
TOPRA Office, 3rd Floor City Reach, 5-6 Greenwich View Place, London, E14 9NN, UK
Day 1 start time: 
13:00 GMT| Day 3 end time: 16:00 GMT
CPD: 15 CPD hours upon successful completion

Who should attend

This course is ideal for:

  • Students of the TOPRA MSc programme
  • Delegates from the regulatory affairs industry who wish to develop their knowledge of the U.S. regulatory environment
  • Delegates from allied industries who wish to have a comprehensive understanding of the subject

What you'll learn

By completing this course, you will be able to:

  • Demonstrate a critical understanding of the U.S. regulatory environment governing drug development and marketing authorisation
  • Interpret and apply FDA regulatory requirements and documentation standards for marketing submissions
  • Critically analyse legal documentation and communications from regulatory bodies such as the FDA
  • Evaluate current research and regulatory developments to make informed, evidence-based judgements in complex situations
  • Communicate regulatory conclusions clearly to both specialist and non-specialist audiences
     

Course overview

A strong grasp of the U.S. regulatory landscape is essential for professionals working in global drug development. This course equips regulatory affairs professionals with a comprehensive understanding of U.S. regulatory operations, including FDA procedures and submission pathways. Through case-based learning, participants will explore how U.S. regulatory practices influence and integrate with global strategies.

Key topics include:

  • The history and legal framework of U.S. drug regulation
  • Common application types (IND, NDA, BLA, ANDA, SNDA) and approval pathways
  • OTC regulation, orphan drugs, and fast-track approvals
  • Effective communication and engagement with the FDA
  • Adverse event reporting, labelling, and advertising controls

Course presenter

TOPRA Masterclasses are developed and delivered by a faculty of expert speakers from relevant industry, agencies, notified bodies and other stakeholders, and are validated by the University of Hertfordshire. 



Pricing

 Standard training course registration fees
 Event Registration Type Price (GBP)
 Standard Price 
 TOPRA Member
£1,750.00 + VAT*
 Standard Price
 Non-member
£2,450.00 + VAT* 
 TOPRA MSc Students
  
£1,750.00 + VAT*









 
Those working for regulatory or government agencies, academic institutions, charities, patient groups, emerging markets, and MSEs (Micro and Small Enterprises) can also access discounted rates by becoming a TOPRA member. For more information about the discounts available, please email meetings@topra.org before making your booking. 

Important Notice On VAT

In compliance with regulations, a *20% VAT will be charged to all attendees, regardless of your country of origin. If you have a VAT number or if the company or organisation you are affiliated with has a VAT number or equivalent please ensure it is visible on your profile. If your VAT number is not visible on your profile, please email finance@topra.org to have it updated. If you do not have a VAT number, there is no action required — VAT will be applied accordingly during the registration process. Please observe that the VAT number needs to be valid.

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Terms and conditions

By booking a place on this course you are agreeing to the Training Terms and Conditions.

 
 
When
24/03/2026 - 26/03/2026
Where
TOPRA 3rd Floor City Reach 5-6 Greenwich View Place London E14 9NN UNITED KINGDOM
Sign in or create an account to register Registration ends 23/03/2026 12:00 (GMT Standard Time)
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