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European
Pharmaceutical
Aerosol Group

We are a voluntary non-profit making consortium of Pharmaceutical Companies.
The member companies develop new products for human use for Pulmonary or Nasal route of delivery intended to be used in the European Market.

Latest News

DDL 2025 EPAG Workshop Overview

The European Pharmaceutical Aerosol Group (EPAG), in collaboration with DDL, hosted the pre-DDL workshop on Wednesday 10th December 2025 at the Edinburgh International Conference Centre.  The Workshop focussed on recent changes in regulatory, academia and science that impact OINDP products. It was a great opportunity for academia and industry to discuss the regulatory changes and their impact. It showcased how EPAG act as an advocacy group to steer efforts accordingly moving forward.

The three hour workshop was free to attend and attracted over 200 of the registered DDL delegates.

  • Dr Tarlochan Singh Purewal presented an overview of EPAG providing a brief history, the vision, objectives, constitution, publications and information on how eligible companies can join EPAG.
  • Three subgroups presented an overview of the purpose, achievements and on-going activities
    • Hlack Mohammed – Impactor Subgroup
    • Paul Kippax – Nasal Subgroup
    • Mark Parry – Dissolution Subgroup
  • There were two invited guest speakers
    • Peter Caspers – as an individual expert.  Peter works at the Dutch Medicines Evaluation Board.  Peter gave an update on EMA Guidelines.
    • Prof. Regina Scherließ – University of Kiel.  Regina presented an overview of work EPAG has supported on Nasal Product Testing – now and in the future. 

The workshop concluded with a Q&A panel discussion featuring the six presenters. Many of the presented materials are available on the EPAG website here (https://epag.co.uk/library/#27-258-wpfd-2025-pre-ddl-workshop)

EPAG Objectives

As defined in our constitution, EPAG will:

  • Focus on Pharmaceutical issues relevant to Pulmonary and Nasal Delivery products, including clinical aspects as appropriate.
  • Establish scientifically based best practices.
  • Provide consensus comment to Industry and Government Agencies to promote safety and quality standards.
  • Recommend harmonised standards and methodology.

We will achieve this by sharing of non-confidential information and by generating our own data through co-operative studies in member companies’ laboratories or sponsored investigations.

Member Companies


Our Vision

The vision for EPAG is that the group will remain the principal industry-based opinion leading and influencing group for the pharmaceutical development and regulation of products for pulmonary and nasal delivery in Europe.

EPAG will continue to be recognised internationally as a valued contributor to the world-wide pulmonary and nasal product development and regulation arena.

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