master class: process development and scale-up in the pharmaceutical industry

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Master Class: Process Development and Scale-Up in the Pharmaceutical Industry School of Chemistry Module CH510 17 and 18 June 2014

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Master Class: Process Development and Scale-Up in the Pharmaceutical Industry. Module CH510 17 and 18 June 2014. School of Chemistry. Process Development and Scale-Up in the Pharmaceutical Industry. - PowerPoint PPT Presentation

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Page 1: Master Class:  Process Development and Scale-Up in the Pharmaceutical Industry

Master Class: Process Development and Scale-Up in the Pharmaceutical Industry

School of ChemistryModule CH510 17 and 18 June 2014

Page 2: Master Class:  Process Development and Scale-Up in the Pharmaceutical Industry

Process Development and Scale-Up in the Pharmaceutical Industry

Dillon Theatre, School of Chemistry 17 and 18 June 2014

As part of their structured PhD programme, NUI Galway’s School of Chemistry, in association with SSPC in UL, are providing a 2-day course on the development and scale-up of organic syntheses for the commercial manufacture of drug substances. The course will

• Focus on synthetic processes for “small molecule” drugs and address the organic,

physical and analytical chemistry involved.

• Cover process selection and development, technology transfer and on-going

optimisation with reference to the safety, environmental, engineering, quality and

regulatory disciplines involved.

• Use real examples to illustrate the subject.

The course will be delivered by

Industrial practitioners

Is aimed at:

PhD students in chemistry and related disciplines.

There will be a fee of €100 for non-NUIG attendees.

Applications to [email protected] (087-6775481)

Page 3: Master Class:  Process Development and Scale-Up in the Pharmaceutical Industry

Process Development and Scale-Up in the Pharmaceutical Industry

Dillon Theatre, School of Chemistry 17 and 18 June 2014

On completion of the course, students will:

• Understand the considerations involved in designing a chemical process suitable for

industrial manufacturing

• Appreciate the scientific disciplines involved in bringing a chemical process from

laboratory to industrial scale

• Be familiar with the organic chemistry involved in the manufacture of some significant

current drugs

• Be able to rationalise and discuss the mechanisms of organic reactions involved in the

synthesis of drugs

• Appreciate the importance of the physical properties of APIs and understand approaches

and techniques for their control

ECTS Credits:

• 5 (on successful completion of assigned course work)

Page 4: Master Class:  Process Development and Scale-Up in the Pharmaceutical Industry

Process Development and Scale-Up in the Pharmaceutical Industry

Dillon Theatre, School of Chemistry 17 and 18 June 2014

Tuesday 17 June

Session 1 Chair Prof Paul V. Murphy (Head of School of Chemistry, NUIG)

09.00 Registration

09.15 Welcome & Introduction Prof Paul V. Murphy (NUIG)

09.30 Process Research and Development. Part 1. Peter J. Harrington (University of Denver)

Synthesis of Lipitor

10.30 Break Tea and coffee (Concourse)

11.00 Process Research and Development. Part 2. Peter J. Harrington

12.00 Technology Transfer to Manufacturing Facility John O’Callaghan (Roche)

Scope and requirements of technology transfer

12.45 Lunch Soup and sandwiches (An Bhialann)

Page 5: Master Class:  Process Development and Scale-Up in the Pharmaceutical Industry

Process Development and Scale-Up in the Pharmaceutical Industry

Dillon Theatre, School of Chemistry 17 and 18 June 2014

Tuesday 17 June

Session 2 Chair Dr Fawaz Aldabbagh (NUI Galway)

13.30 Quality Assurance Clare Desbonnet (Roche)

Regulatory obligations

Process validation

14.30 Analytical Controls Patricia Clancy (Roche)

Specifications and test methods for drug substances

In-process controls and process analytical technology (PAT)

15.30 Break Tea and coffee (Concourse)

16.00 Chemical Engineering Aspects Eoin Cleary (Roche)

Selection and sizing of equipment

Process flow and process “fits”

17.00 Process safety management Bill Fleming (Fleming Professional)

Risk identification

Quantified risk assessment

18.00 Close

Page 6: Master Class:  Process Development and Scale-Up in the Pharmaceutical Industry

Process Development and Scale-Up in the Pharmaceutical Industry

Dillon Theatre, School of Chemistry 17 and 18 June 2014

Wednesday 18 June

Session 3 Chair Dr Niall Geraghty (NUI Galway)

9.00 Safety Testing Michael Kennedy (SPDS Ltd)

Chemical reaction hazard assessment

Dust and electrostatic hazard assessment

Vent sizing

10.00 Environmental Management Seamus O’Grady (Roche)

Licence requirements (ELVs)

Waste minimisation

11.00 Break Tea and coffee (Concourse)

11.30 Process Optimisation at the Manufacturing Facility Dennis Smith (NUIG)

Approaches to on-going development

Case study - Mycophenolate Mofetil

12.30 Lunch Soup and sandwiches (An Bhialann)

Page 7: Master Class:  Process Development and Scale-Up in the Pharmaceutical Industry

Process Development and Scale-Up in the Pharmaceutical Industry

Dillon Theatre, School of Chemistry 17 and 18 June 2014

Wednesday 18 June

Session 4 Prof Kieran Hodnett (UL/SSPC)

13.30 Solid State Properties of APIs Denise Croker (UL)

Critical properties and test methods

14.15 Solid state properties and manufacturing John Collins (UL/SSPC)

The impact of solid state properties on operations

Operational technologies for control of solid state properties

15.15 Break Tea and coffee (Concourse)

15.30 Crystallisation and control of solid state properties Mark Barrett (APC/SSPC)

16.30 Case studies of process and product quality improvements arising from

crystallisation optimisation John O’Reilly (Roche)

17.30 Close