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Expertise

• Oral Drug Delivery
• DMPK Consultancy and Dose Selection
• Pharmacokinetic Modelling
• Complex Medicines
• Paediatric Product Development
• CMC Regulatory
• Clinical Pharmacology

Presentations

• Clinically-relevant dissolution specifications, implication for use in the post-approval setting & tension with F2 similarity testing
• Transforming promising molecules into valued medicines – the emerging Alderley Park Translational Science Ecosytem (APTrans)
• Design space considerations for dissolution methods
• Accelerating the development of drug products using advanced pharmaceutical design tools and manufacturing
• Pharmaceutical Quality: The dissolution test and clinically relevant specifications – impact on product development
• Clinically relevant specifications in practice: What have we learned since the QbD Pilot Program?
• Introduction to the Biopharmaceutics Risk Assessment Roadmap (BioRAM), Drug Delivery Scenarios and Scoring Grid
• Score sheet, Box 1: Early basic knowledge, starting point.  From Blueprint to action: Getting to critical questions and knowledge.
• BioRAM: connecting the drug product with the patient – from design to optimized product
• In silico modelling: Subcutaneous Bioavailability of mAbs
• Biopharmaceutics in Complex Parenteral Formulation Design
• It’s all in the delivery
• Early understanding of PK/PD: setting up success in development?
• It’s never too early to put the patient first
• Streamlined pathways to clinical success through integrated modelling
• Physiologically-based biopharmaceutics modelling for nasal delivery
• Formulations – what’s new and do I need to be there?
• Paul Dickinson From AZ to CRO Founder

Awards and Recognition

• King's Award for Enterprise
• Bionow Business Growth Award
• Medilink North of England Export Achievement Award
• Life Sciences Innovator: Application, Product & Service Design
• OBN Best CRO Award
• Bionow Technical Services Award Winner

Categories

• Panel Discussions
• Podcasts
• Invited talks and podium presentations