The Making Pharmaceuticals conference programme is free to attend, with parallel conference streams, giving visitors a huge choice of topics.
Most sessions run in parallel so you can move between the different conference rooms, creating your own tailored conference programme to suit your interests and professional information requirements.

If you would like to be involved in this year’s programme, please contact Victoria Emerton.

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26 April

Room A

9:30 am

Using Digital Data and Analytics to Problem Solve When Manufacturing Pharmaceuticals

Speaker

9:50 am

Project Management to Enable Digitalisation – How can Project Managers Deliver Projects Which are Future Proofed for New Digital Incentives.

Speaker

10:10 am

Impact of Climate Change on Pharmaceutical Manufacture

Speaker

10:30 am

Break

11:30 am

Serialisation Operating Models for Different Supply Chain Partners

Speaker

11:50 am

Names, Logos, Branding, Regulated Content – How do you develop your packaging artwork for launch?

Speaker

12:10 pm

The Impact of Electronic Patient Leaflets on Information Management and Product Supply

Speaker

12:50 pm

Child Safe Packaging and the Impact on the Eldery

Speaker

1:10 pm

Break

2:00 pm

3:00 pm

Break

3:45 pm

APS Emerging Technologies Focus Group

Speakers

  • Prof Clive Roberts Vice Chairman - Academy of Pharmaceutical Sciences Emerging Technologies Focus Group
  • Dr Dimitrios Lamprou Reader in Pharmaceutical Engineering - Queens University Belfast

3:55 pm

Emerging Technologies in Pharmaceutical Manufacturing

Speaker

4:15 pm

The Potential for Additive Manufacturing in Pharmaceutical Production

Speaker

Room B

9:30 am

Combatting the COVID-19 Pandemic – The Role of Phospholipids

Speaker

9:50 am

EfferShield: A Disruptive Innovation for Manufacturing and Packaging of Effervescent Products

Speaker

10:10 am

Introduction to Down Streaming Using HPMCAS

Speaker

  • Shilpa Mistry Head of Pharma,UK and Ireland - Chemlink Specialities

10:30 am

Break

11:30 am

Strategic API Procurement – How to Choose a Source That is Right for You

Speaker

  • Nick Carter Director / GDP Designated Person - Wessex Fine Chemicals

11:50 am

12:10 pm

12:30 pm

Break

2:00 pm

3:00 pm

Break

3:45 pm

Introducing UltraBurst™ a Novel Excipient that Addresses the 3 Most Important Success Factors for ODTs

Speaker

4:05 pm

Air and Water Microbial Monitoring

Speaker

  • John Cobb Company Microbiologist - PMT (GB) Ltd

4:25 pm

Digitalising Line Clearance – Presentation Summary

Speaker

Room C

10:00 am

 Healthcare Distribution Challenges with GDP Regulations during the Pandemic

Speaker

  • Geoff Mellor Technical Director - Healthcare Distribution Association UK

10:30 am

Break

11:30 am

MMCS – Introducing a New Route to Pharma GDP Compliance and Standardisation

[view]

Speakers

12:30 pm

Workshop: MMCS – Introducing a New Route to Pharma GDP Compliance and Standardisation

Speakers

Break

2:00 pm

3:00 pm

Break

3:45 pm

Quality Risk Management in GDP

Speaker

  • Neil Wayman Secretary - Pharmaceutical Quality Group (PQG)

Room D

9:30 am

A Guide to Outsourced Stability Storage

[view]

Speaker

  • Wendy Cullen Head of UK Sales - Stability Storage - Source Bioscience

10:30 am

Break

11:30 am

Biopharma’s Growth Story: Ten Key Themes

Speaker

  • Dr Duncan Emerton Executive Director, Custom Intelligence & Analytics - Informa Pharma Intelligence

12:00 pm

How to Effectively Manage a Remediation Programme and Sustain Quality Improvements’

Speaker

1:00 pm

Break

2:00 pm

3:00 pm

Break

3:45 pm

IP Protection in the Life Sciences – AI, 5G, AM and Beyond

Speaker

4:05 pm

Formulating Pharmacokinetics

Speaker

4:25 pm

Marketing LifeSciences; Successes and Learnings

Speaker

Room E

9:30 am

What are the Differences in Responsibilities Between a RP, QP & RPi?

Speaker

10:10 am

The Cleaning Challenge with Pharma Excipients

[view]

Speaker

10:30 am

Break

11:30 am

Digitalisation to Improve Knowledge Management

Speaker

12:10 pm

Process Vessel Temperature Control Systems (How to Reduce Operational Costs and Improve Controllability)

Speaker

12:30 pm

Break

2:00 pm

3:00 pm

Break

3:45 pm

Collaborative Innovation to Drive Progress- How Can Working With Others Speed up Your Innovation

Speaker

  • Dr Dave Berry Grand Challenge and Digital Strategy Lead - Centre for Process Innovation

27 April

Room A

9:15 am

Failures in the Temperature-Controlled Supply Chain – An Auditor’s Experiences

Speaker

  • Bob Hayes Vice-Chair, Pharmaceuticals Technical Activities Committee - Institution of Mechanical Engineers

9:35 am

Design for Successful Validation

Speaker

  • Bob Hayes Vice-Chair, Pharmaceuticals Technical Activities Committee - Institution of Mechanical Engineers

9:55 am

Managing Change – Control The Risk!

Speaker

10:15 am

Break

11:30 am

Surface Engineering Approaches to Control Biological – Surface Interactions

Speaker

  • Dr Paul Roach Reader in Biomaterials and Interface Science - Loughborough University

12:00 pm

Electrospinning: an Emerging Medicines Manufacturing Method

Speaker

12:30 pm

Break

2:00 pm

Excipient Sustainability : A User and Supplier’s Perspective

Speaker

2:20 pm

Best Practices Guide for the Safety Evaluation of “Novel” Pharmaceutical Excipients with Reference to the IPEC Safety Guide

Speaker

2:40 pm

Excipient Selection for Paediatric Medicines Using a Risk/Benefit Approach

Speaker

Room B

9:15 am

Particle Size Analysis Basics For Pharmaceutical Ingredients and Formulations

Speaker

  • Andy Keating Sector Sales Manager - Life Sciences - HORIBA UK LTD

9:35 am

Nutritional Solutions to Support Cancer Treatment

Speaker

  • Barbara Troesch Senior Scientific Affairs Manager Global Pharma Solutions & Clinical Nutrition - DSM Nutriitional Products

9:55 am

Continuous Manufacturing of Pharmaceutical Nanoparticles (CM-NANO)

Speaker

  • Dr Luis Padrela Lecturer - Synthesis & Solid State Pharmaceutical Centre (SSPC), University of Limerick

10:15 am

Break

11:30 am

Compaction Simulators : A Material-sparing Method to Accelerate Tablet Formulation Development

Speaker

11:50 am

Overcoming the Challenges During Tableting

Speaker

  • Shilpa Mistry Head of Pharma,UK and Ireland - Chemlink Specialities

12:10 pm

Harnessing Raman Imaging to Boost Pharmaceutical Product Analysis, From Formulation to QC

Speaker

12:30 pm

Break

2:00 pm

The Guide to GMP

[view]

Speaker

2:20 pm

Ratio Calibration Procedure for Enhanced Accuracy and Ease of Determination of Residual Oxygen in Nitrogen Purged Pharmaceutical Packaging

Speaker

  • Frank Judge Consultant Chemist - Butterworth Laboratories

2:40 pm

Data Integrity Maturity Assessments – Trends and Tools

Speaker

  • David Thompson Principal Consultant - Clarity Compliance Solutions Ltd

Room C

9:15 am

Introduction to MTRC at ARU

Speaker

  • Prof. Selim Cellek Director of the Medical Technology Research Centre - Anglia Ruskin University

9:20 am

Novel Therapies for Cataract

Speaker

  • Prof. Barbara Pierscionek Deputy Dean (Research and Innovation), Faculty of Health, Education, Medicine and Social Care - Anglia Ruskin University

9:40 am

Inhibiting DNA Repair in Human Cancer Cells

Speaker

  • Prof. Chris Parris Head of the School of Life Sciences in the Faculty of Science and Engineering - Anglia Ruskin University

10:00 am

Novel Nanomedicines for Cancer Therapy

Speaker

10:15 am

Break

10:20 am

Discovery of Novel Anti-fibrotic Drugs Through Phenotypic Screening

Speaker

  • Prof. Selim Cellek Director of the Medical Technology Research Centre - Anglia Ruskin University

11:30 am

E-PILs, What are They and What are the Opportunities to the Industry?

Speaker

11:50 am

Artwork and Content Management; Feeding the e-PI Process and Delivering Exceptional Content Quality

Speaker

12:10 pm

The Art of the Possible

Speaker

12:30 pm

Break

2:00 pm

When Clean Means Corrosion

Speaker

2:20 pm

Smart Factory: Practical Examples

[view]

Speaker

  • Mark Yeeles VP Industrial Automation UK&I - Schneider Electric

Room D

9:15 am

How to Approve EXCiPACT as a 3rd Part Audit Provider

Speaker

9:35 am

Application of EXCiPACT GMP to Excipient-like Materials Used in Pharmaceutical Drug Product Manufacture

Speaker

10:45 am

Break

12:00 pm

GAMP 5 and Data Integrity – Trends for Manufacturing Systems

[view]

Speaker

  • Hilary Mills-Baker European Quality and Validation Manager - Emerson Automation Solutions

12:30 pm

Break

2:00 pm

Dessicants and Sustainability in Active Packaging

Speaker

2:20 pm

Driving GDP Compliance for Outsourced Logistics Activities

Speaker

2:40 pm

Why the Future is Flexible in CDMOs

[view]

Speaker

Room E

9:15 am

Common GMP Deficiencies

Speakers

9:45 am

Common GDP Deficiencies

[view]

Speakers

10:15 am

Break

11:30 am

Quality Risk Management in GDP

Speaker

  • Neil Wayman Secretary - Pharmaceutical Quality Group (PQG)

12:30 pm

Break

3:20 pm

Break