Regulatory: Pharma

Training format

Topic

  • Next: 16-17 Mar 2026 Live online
  • Also: 30 Sep-1 Oct 2026 Live online

Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Application

Live online

This seminar looks at the latest guidance on how to prepare a clinical overview and summary in accordance with regulatory expectations and to comply with the requirements of the Common Technical Document (CTD).

  • 6 CPD hours Focused
  • Presented by Dr John Price
  • Next: 4 Mar 2026 Live online
  • Also: 6 Oct 2026 Live online
  • Trending

Orphan Drug Regulatory Masterclass: EU & US Insights

Live online

This must-attend event will provide an essential overview of the opportunities and challenges presented by orphan drug regulation.

  • 6 CPD hours Focused
  • Presented by Shaun Stapleton
  • Next: 24-25 Sep 2026 Live online

The FDA Drug Approval Process

Live online

A comprehensive overview of FDA procedures, requirements for marketing authorisations and recent developments affecting the drug approval process in the US

  • 12 CPD hours Focused
  • Presented by Andrew Willis
  • Next: 2-3 Jun 2026 Live online
  • Also: 11-12 Nov 2026 Live online

Variations to Marketing Authorisations

Live online

A two-day event that will provide an invaluable overview of the EU system for variations, with practical advice on the preparation and submission of variation applications using the various European procedures.

  • 12 CPD hours Focused
  • Presented by Andrew Willis
  • Next: 23-24 Apr 2026 Live online
  • Also: 19-20 Oct 2026 Live online

Chemistry, Manufacture and Control (CMC) - Regulatory Requirements for Biological Drug Products

Live online

The regulatory requirements for Biological drug products are complex, and pharmaceutical companies are continuously under pressure to ensure regulatory compliance from drug discovery to post-marketing surveillance. This course has been designed to help you navigate the complex regulatory requirements for biological drugs, including ATMPs. It will clearly depict the differences between small and large molecules and the development approaches which reflect the type of molecule. It will address the key aspects of the CTD, look at the CMC regulatory requirements during different stages of development, and discuss the importance of change control.

  • 12 CPD hours Focused
  • Presented by Andrew Willis
  • Next: 10 Jun 2026 Live online
  • Also: 9 Dec 2026 Live online

Antimicrobial Resistance (AMR) and 'One Health': Current Challenges, Regulatory Frontiers and Future Solutions

New for 2026

Live online

This course will allow participants to explore the regulatory landscapes governing AMR, discover innovative solutions and understand the challenges AMR poses across different sectors.

  • 6 CPD hours Focused
  • Presented by Linda Oyama
  • Next: 15 Jul 2026 Live online

Understanding Toxicology: A Guide for Non-Toxicologists

New for 2026

Live online

This introductory course provides a clear and practical foundation in toxicology. It covers key principles, terminology and testing methods, helping participants confidently interpret and apply toxicological data in chemical safety and compliance contexts.

  • 3 CPD hours Masterclass
  • Presented by Laura Robinson
  • Next: 23 Jun 2026 Live online
  • Also: 4 Dec 2026 Live online

Digital CMC: The Key To Realising Pharma 4.0

New for 2026

Live online

Whether you’re looking to optimise existing processes or lay groundwork for a digital transformation, the course will teach the tools to leverage Digital CMC as a cornerstone of Pharma 4.0 success.

  • 6 CPD hours
  • Presented by Lewis Shipp
  • Next: 20-21 Apr 2026 Live online
  • Also: 12-13 Oct 2026 Live online

The Regulatory Requirements on Nitrosamines in the Pharmaceutical Industry

Live online

In this webinar, we will discuss the major requirements and strategies for nitrosamines, a hot topic that is on the forefront of many company's minds.

  • 6 CPD hours Focused
  • Presented by Jason Brown