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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
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Organized by:
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Royal Pharmaceutical Society |
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Invited Speakers:
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David Littlejohn, Andrew Phillips, David Elder, Bronwyn Phillips, Tran Pham, Matthew Bloomfield, Helen Williams, Ben Rackstraw,
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Deadline for Abstracts:
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Friday 19 November 2010
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Registration:
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09.30
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E-mail:
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events@rpsgb.org
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