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The future of small molecule development is being redefined. But with innovation comes complexity including formulation challenges, developability roadblocks, tight timelines and limited resources. For early-stage pharma companies, the stakes are high; missteps can lead to costly delays, regulatory setbacks, and missed market opportunities.  
  
Discover strategies with the industry experts as we break down the critical phases of small molecule development, covering formulation strategies, manufacturing solutions, and CMC best practices to accelerate your path to the clinic. Beyond the science, we’ll tackle the drug development business, including aligning with investor expectations and securing funding in a competitive landscape. 

Join us in London to gain the insights, tools, and connections you need to de-risk development, optimize your strategy, and fast-track your innovation to market success. Plus, take advantage of exclusive 1:1 office hour with our experts to discuss your molecule challenges.  

Who Should Attend 

Ideal for emerging pharma startups seeking to accelerate clinical entry and deliver innovative medicines to patients faster. Suited for professionals in Preclinical & Formulation Development, CMC, Drug Substance & Product Development, Project Management, Manufacturing & Operations, Supply Chain Management, as well as pharma consultants seeking a CDMO partner for developing and manufacturing oral solid dosage forms.  

Agenda:

 

 TIME

AGENDA 

SPEAKERS 

10:00 am – 10:45 am 

Breakfast & Registration 

 

10:45 am – 11:00 am 

Welcome Note 

Matthew Streeter  

General Manager,  

Catalent Nottingham 

 

Matt Ling (moderator)   

Director, Scientific Services, Catalent Nottingham 

11:00 am – 11:30 am 

Formulating in Early Discovery: 

Embedding Formulation Considerations into Hit-To-Lead Optimization 

David Pearson  

Director of Form and Formulation, Sygnature Discovery  

11:30 am – 12:00 pm 

Formulating with Less API:  

Application of API Sparing Techniques in Oral Drug Development 

Karl Box

Chief Scientific Officer, 

Pion Inc 

12:00 pm – 1:00 pm 

Power Lunch  

 

1:00 pm – 1:30 pm 

Formulating for Success:  

Early-Phase Strategies to Avoid Costly Setbacks 

Stephen Tindal

Director, Scientific Advisory, Europe, Catalent 

1:30 pm – 2:00 pm 

Manufacturing Insight: 

Lessons from 12 Years of the Manufacturing Classification System 

Kendal Pitt

Visiting Professor, University of Strathclyde & Honorary Professor, Leicester School of Pharmacy, De Montfort University 

2:00 pm – 2:30 pm 

Refresh & Recharge 

 

2:30 pm – 3:00 pm 

Fast-Tracking Clinical Development:  

Navigating UK Clinical Trial Regulations to Reduce Risk and Accelerate Timelines 

Karen Chalk

Head of Clinical Project Management & Regulatory Affairs, HMR 

 

Sally Dowen

Director, Lealto Consulting 

3:00 pm – 3:30 pm 

Founder's Insight:  

Tackling Early Drug Development Challenges with Strategic Partners That Deliver 

Emilia Neuwirt

Co-Founder, CEO 

EMUNO Therapeutics  

3:30 pm – 4:15 pm 

Panel Discussion:  

Securing Capital in a Competitive Market - What Early-Stage Pharma Needs to Know 

Ronak Savla  

Director, Strategic Ventures, Catalent 

 

Graham Mills

Principal, Abingworth  

 

Owen Smith

Partner, 4BIO Capital  

 

Angelos Georgakis

Executive Coach to Biotech Leaders  

 

Jack O’Meara

CEO of Helicon 

 

4:15 pm – 5:00 pm  

Closing & Networking Cocktail 

Sherief Shaaban

VP and Chief Commercial Officer, Catalent

ABOUT CATALENT NOTTINGHAM 
 
Catalent’s Nottingham facility focuses on early-stage development of small molecule drug candidates from the bench to clinic.  This facility offers an array of services that support oral dosage forms that include characterization, formulation and analytical development, manufacturing and clinical packaging, labelling and worldwide distribution.  Our Nottingham location is the home of our bioavailability enhancement technologies, including Catalent Spray Drying and Hot Melt Extrusion to support the needs of our client’s most challenging compounds. This MHRA approved facility includes cGMP dose form manufacturing, packaging, analytical and development laboratories with OEB 1-3 and controlled drug storage to handle even your most challenging products
 

Registration: Free to attend, please sign up via this link.

Contact
Phone: 01223 896450
Phone: 01223 896456

Accelerate Small Molecule Development with Smart Formulation & Funding Strategies

Wednesday 4 June 2025, 10.00 - 17.00
4 June 2025 10:00
Royal Society of Chemistry
Burlington House
Piccadilly
London, London W1J 0BA
United Kingdom