Ian Ragan

Drivers and barriers in the consistency approach for vaccine batch release testing: Report of an international workshop.

Rob J Vandebriel, Martijn W P Bruysters, Marie-Jeanne Schiffelers, 2017, Biologicals : journal of the International Association of Biological Standardization.

Advancing the 3Rs in regulatory toxicology - Carcinogenicity testing: Scope for harmonisation and advancing the 3Rs in regulated sectors of the European Union.

Rick Clayton, Mattias Öberg, Jan Willem van der Laan, 2014, Regulatory toxicology and pharmacology : RTP.

Preclinical development of monoclonal antibodies

Ian Ragan, Kathryn Chapman, Colin Green, 2009, mAbs.

Waiving in vivo studies for monoclonal antibody biosimilar development: National and global challenges

Jennifer Sims, Ian Ragan, Kathryn Chapman, 2016, mAbs.

Steps towards the international regulatory acceptance of non‐animal methodology in safety assessment

Fiona Sewell, Natalie Burden, Nichola Gellatly, 2017, Regulatory toxicology and pharmacology : RTP.

A global initiative to refine acute inhalation studies through the use of 'evident toxicity' as an endpoint: Towards adoption of the fixed concentration procedure.

Hajime Kojima, Fiona Sewell, Kyuhong Lee, 2015, Regulatory toxicology and pharmacology : RTP.

Recommendations from a global cross-company data sharing initiative on the incorporation of recovery phase animals in safety assessment studies to support first-in-human clinical trials.

Fiona Sewell, Sally Robinson, Beatriz Silva Lima, 2014, Regulatory toxicology and pharmacology : RTP.