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Publications

Research Papers and Book Chapters

Dec 2020

Predicting bioavailability of monoclonal antibodies after subcutaneous administration: Open innovation challenge

SEDA author(s): C. Patterson

Date: Dec 2020

Published: Advanced Drug Delivery Reviews

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Dec 2018

Effect of multiple-dose osimertinib on the pharmacokinetics of simvastatin and rosuvastatin

SEDA author(s): P.A. Dickinson

Date: Dec 2018

Published: British Journal of Clinical Pharmacology

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Jun 2018

The effect of itraconazole and rifampicin on the pharmacokinetics of osimertinib

SEDA author(s): P.A. Dickinson

Date: Jun 2018

Published: British Journal of Clinical Pharmacology

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May 2018

Nonclinical safety and pharmacokinetics of Miglyol 812: A medium chain triglyceride in exenatide once weekly suspension

SEDA author(s): C. Patterson

Date: May 2018

Published: Journal of Applied Toxicology

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Apr 2018

Sep 2017

Nov 2016

Sep 2016

Asymmetric Distribution in Twin Screw Granulation

SEDA author(s): M. de Matas

Date: Sep 2016

Published: European Journal of Pharmaceutics and Biopharmaceutics

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Aug 2016

Jul 2016

Strategic framework for education and training in quality by design (QbD) and process analytical technology (PAT)

SEDA author(s): M. de Matas

Date: Jul 2016

Published: European Journal of Pharmaceutical Sciences

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May 2016

Jan 2016

Clinically Relevant Dissolution for Low-Solubility Immediate-Release Products

SEDA author(s): P.A. Dickinson, P. Stott

Date: Jan 2016

Published: Poorly Soluble Drugs: Dissolution and Drug Release.

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Invited Talks and Podium Presentations

Nov 2020

It’s all in the delivery

SEDA author(s): P. Stott

Date: Nov 2020

Published: Bio Integrates 2020, Digital Event

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Nov 2020

Biopharmaceutics in Complex Parenteral Formulation Design

SEDA author(s): C. Patterson

Date: Nov 2020

Published: 2020 Bionow Oncology Conference, Digital Event

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Jun 2020

In silico modelling: Subcutaneous Bioavailability of mAbs

SEDA author(s): C. Patterson

Date: Jun 2020

Published: In Roundtable: "Predicting Bioavailability of Monoclonal Antibodies after Subcutaneous Administration: Open Innovation Challenge. CRS Virtual Annual Meeting

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Sep 2017

BioRAM: connecting the drug product with the patient – from design to optimized product

SEDA author(s): P.A. Dickinson

Date: Sep 2017

Published: The 8th APS International PharmSci Conference, University of Hertfordshire, Hatfield, UK

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Jul 2017

Score sheet, Box 1: Early basic knowledge, starting point.  From Blueprint to action: Getting to critical questions and knowledge.

SEDA author(s): P.A. Dickinson

Date: Jul 2017

Published: Applying the Biopharmaceutics Risk Assessment Roadmap (BioRAM): Patient-Focused Drug Development: Developing critical knowledge with BioRAM and the BioRAM Scoring Grid.The USP Meetings Center in Rockville, MD, USA

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Oct 2016

Introduction to the Biopharmaceutics Risk Assessment Roadmap (BioRAM), Drug Delivery Scenarios and Scoring Grid

SEDA author(s): P.A. Dickinson

Date: Oct 2016

Published: EuPAT8, University College Cork, Cork, Ireland

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Oct 2015

Clinically relevant specifications in practice: What have we learned since the QbD Pilot Program?

SEDA author(s): P.A. Dickinson

Date: Oct 2015

Published: In Roundtable: Clinically Relevant Specifications: Where Are We Now? AAPS Annual Meeting, Orange County Convention Center, Orlando, Fl, USA

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Oct 2015

Pharmaceutical Quality: The dissolution test and clinically relevant specifications – impact on product development

SEDA author(s): P.A. Dickinson

Date: Oct 2015

Published: International Multidisciplinary Symposium on Drug Research and Development, Anadolu University, Eskişehir, Turkey

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Oct 2015

Accelerating the development of drug products using advanced pharmaceutical design tools and manufacturing

SEDA author(s): M. de Matas

Date: Oct 2015

Published: International Multidisciplinary Symposium on Drug Research and Development, Anadolu University, Eskişehir, Turkey

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Sep 2015

Design space considerations for dissolution methods

SEDA author(s): P.A. Dickinson

Date: Sep 2015

Published: Joint Pharmaceutical Analysis Group Symposium on the Impact of emerging regulatory guidelines on development and commercial activities at PharmSci 2015, East Midlands Conference Centre, Nottingham, UK

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Sep 2015

Transforming promising molecules into valued medicines – the emerging Alderley Park Translational Science Ecosytem (APTrans)

SEDA author(s): M. de Matas

Date: Sep 2015

Published: PharmSci 2015, East Midlands Conference Centre, Nottingham, UK

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Posters and Abstracts

Nov 2018

Analysis of patient derived xenograft studies in Oncology drug development: impact on design and interpretation of future studies

SEDA author(s): J. Dickinson, M. de Matas, P.A. Dickinson

Date: Nov 2018

Published: PKUK, Midland Hotel, Manchester, UK

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