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Characterisation of active product ingredients

 
  September 17, 2010  
     
 
Royal Pharmaceutical Society, London
Thursday 2 December 2010


09.30 Registration and coffee

0955 Introduction

Ken Leiper, Chairman, Joint Pharmaceutical Analysis Group

10.00 Use of spectroscopic techniques for particle characterisation during drying of pharmaceutical APIs

Prof David Littlejohn, University of Strathclyde and CPACT

10.40 The use of NMR to monitor trace and genotoxic impurities

Dr Andrew Phillips, AZ

11.15 Short break (no refreshment)

11.25 Generic methods for determining genotoxic impurities

Dr David Elder, GSK

12.00 Securing GMP compliance of the API supply chain

Bronwyn Phillips, MHRA

12.35 Lunch, exhibition and poster viewing**

13.50 Solid-state NMR applications to structural characterisation and quantitative analysis of APIs

Dr Tran Pham, GSK

14.25 Transmission Raman spectroscopy for the analysis of crystalline and amorphous forms of APIs

Dr Matthew Bloomfield, Cobalt Systems

15.00 Tea break

15.25 Understanding API degradation pathways using electron paramagnetic resonance spectroscopy

Helen Williams, AZ

16.05 Common deficiencies in the API section of the quality dossier

Dr Ben Rackstraw, MHRA

16.35 Closing remarks

16.45 Close

 
 
Organized by: Royal Pharmaceutical Society
Invited Speakers:

David Littlejohn,

Andrew Phillips,

David Elder,

Bronwyn Phillips,

Tran Pham,

Matthew Bloomfield,

Helen Williams,

Ben Rackstraw,

 

 
Deadline for Abstracts: Friday 19 November 2010
 
Registration: 09.30
E-mail: events@rpsgb.org
 
   
 
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