PANEL SESSION:

North East Pharmaceutical Manufacturing Showcase – leading the way in flow chemistry & continuous processing

Time & Location

Wednesday: 14.00 to 15.00, Stage 3

Session Host

NEPIC

About this Session

In this session, NEPIC will bring together some key players from the North East pharmaceutical cluster to discuss the strengths of pharma manufacturing within the region. We will be joined by NEPIC member companies to discuss their journeys within the sector, as well as key challenges, opportunities, technology trends and synergies with the chemical sector. A particular focus will be placed on the role of continuous processing, as this is one of the key areas of innovation within the pharma manufacturing space. This will be a great opportunity to find out more about a regional sector that contributes a third of the UK’s pharmaceutical GDP.

Session Host: Ryan Siddall, Head of Technical, North East Process Industry Cluster (NEPIC)

Panellists/Presentation Title:

James Rogers, Site Head, Sterling Pharma Solutions
The Role of flow in environmental sustainability
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Will Reynolds, Flow Chemistry Development Chemist, Sterling Pharma Solutions
The Role of flow in environmental sustainability
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Stephen Byard, Principal Research Fellow, Science & Technology, Candidate Development, Quotient Sciences
Translational Pharmaceutics®: Accelerating Synthesis to Clinic and Beyond
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Christine Gardner, Inspection and Packaging Technical Lead, GSK
GSK Barnard Castle the future is bright…..
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Dr. Charles Heiss, Associate Director – Fujifilm Diosynth Biotechnologies
FUJIFILM Diosynth Biotechnologies capabilities and the MaruXTM continuous biomanufacturing platform

Continuous manufacturing provides a solution for uncertainty in capacity as drug candidates progress through clinical development to commercial supply. However, adoption has been slow due to technical and operational challenges associated with managing large liquid volumes, integration of unit operations, and environmental and process controls. We have executed the successful production of a monoclonal antibody using a 500 L scale connected process with a single-use flow path in a non-GMP pilot facility, which is a forerunner to the construction of flexible continuous GMP manufacturing facilities.

Ryan Siddall

Ryan Siddall

Head of Technical, North East Process Industry Cluster (NEPIC)

James Rogers

James Rogers

Site Head, Sterling Pharma Solutions

Will Reynolds

Will Reynolds

Flow Chemistry Development Chemist, Sterling Pharma Solutions

Stephen Byard

Stephen Byard

Principal Research Fellow, Science & Technology, Candidate Development, Quotient Sciences

Christine Gardner

Christine Gardner

Inspection and Packaging Technical Lead, GSK

Dr. Charles Heise

Dr. Charles Heise

Associate Director - Fujifilm Diosynth Biotechnologies

Charles Heise is Associate Director in the Bioprocessing Strategy & Development group at FUJIFILM Diosynth Biotechnologies working on developing connected, integrated processes.  He has 15 years of experience in leading the development and scale up of manufacturing processes for clinical and commercial stage biologics. He is co-inventor of the award winning SymphonXTM purification skid and the downstream technical lead for FDB’s continuous biomanufacturing process (MaruXTM). Charles has contributed to biopharma industry publications on continuous manufacturing roadmapping.