Designing Better Pediatric Medicines: Strategies to meet patient needs and regulatory expectations in the development of acceptable age-appropriate dosage forms

London, United Kingdom | 18 March 2026
Overview

Join us for a full-day event dedicated to advancing pediatric medicine, featuring expert-led sessions and networking opportunities. 

Hosted by the Quotient Sciences team, this event brings together leading professionals to discuss key topics in pediatric drug development, including taste and palatability assessments, regulatory considerations, food compatibility, formulation development, and patient acceptability.

The agenda includes presentations from renowned speakers, interactive Q&A sessions, and ample time for networking over lunch and a drinks reception. Whether you’re looking to deepen your expertise, connect with peers, or explore the latest innovations in pediatric science, this event promises valuable insights and engaging discussions.

  • Key learning objectives
  • Taste and palatability assessment approaches for pediatric dosage forms
  • Regulatory perspectives on PIP/PSP, pediatric QTPP, and excipient risk assessment  
  • Pediatric biopharmaceutics considerations  
  • Food compatibility in pediatric studies
  • Formulation development pathways for pediatric products
  • Patientcentric design and acceptability in hospital settings  

 

TimeDescription
09:00 AM - 5:00 PMDuration
09:00 AM – 09:15 AMWelcome & Introduction - Nazim Kanji
09:15 AM – 10:00 AMJenny Walsh (Jenny Walsh Consulting) Topics: Pediatric Quality Target Product Profiles Q&A
10:00 AM – 10:45 AMKingsley Iyoha (Quotient) Topic: Pediatric Formulation Development and Clinical Assessment Q&A
10:45 AM – 11:00 AMCoffee Break
11:00 AM – 11:45 AMEnosh Mwesigwa (Azelis Pharma and Healthcare) Topic: Flavour Masking of Pediatric Formulations Q&A
11:45 AM – 12:30 PMCatherine Tuleu (UCL) Topic: Taste/Palatability Assessments Q&A
12:30 PM – 13.15 PMJustin Holland (Quotient) Topic: Food Compatibility Studies Q&A
13.15 PM – 2:00 PMLunch & Networking
2:00 PM – 2.45 PMLouise Bracken (Alder Hey Children’s Hospital) Topics:Patient Considerations for Pediatric Dosage Form Design(TBC) Pediatric Acceptability Q&A
2:45 PM – 3.30 PMHannah Batchelor (Strathclyde University) Topic: Pediatric Biopharmaceutics Q&A
3.30 PM – 5:00 PMDrinks reception | Closing Remarks Open floor for questions

 

Register
Location
Royal Society of Chemistry
Burlington House, Piccadilly, W1J 0BA
London, United Kingdom

Meet our experts:

We look forward to meeting you at the seminar.

Nazim Kanji

Executive Director, Pediatric Services

Nazim Kanji has over 25 years of experience in the pharmaceutical and consumer healthcare industries, where he has worked in produ...

About Nazim
Dr. Catherine Tuleu

Professor in Paediatric Pharmaceutics at UCL School of Pharmacy

Catherine Tuleu, research, inherently translational, ranges from formulation, methodology development to clinical implementation, ...

About Catherine
Jenny Walsh

Pharmaceutical Development Consultant and Director at Jenny Walsh Consulting Ltd

Jenny Walsh has over 30 years’ experience in the Pharmaceutical and Consumer Healthcare Industry and has been an independent consu...

About Jenny
Hannah Batchelor

Strathclyde Institute of Pharmacy and Biomedical Sciences Director of Research

Professor Hannah Batchelor specialises in developing medicines tailored to the needs of children, with a particular focus on ageap...

About Hannah
Kingsley Iyoha

Senior Director, Development, Formulation Development

Kingsley has over 20 years’ experience in product development within the pharmaceutical and consumer healthcare industries, includ...

About Kingsley
Justin Holland

Executive Director, UK Analytical, Analytical Development

Justin Holland has over 20 years of experience in pharmaceutical testing to support all phases of drug product development from pr...

About Justin
Enosh Mwesigwa PhD MBA CInP

Azelis Pharma and Healthcare

About Enosh

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