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HUM-MOLGEN
-> Events
-> Courses and Workshops |
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August 10, 2007 |
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PharmaTraining Services, London UK
11 & 12 October 2007
Day 1
9.00 Registration
9.30 Introduction
9.45 Solubility, absorption and bioavailability
– an introduction
10.45 Break
11.15 The gastro-intestinal tract in relation to drug
absorption
12.15 Introduction to salts and physical form
(polymorphism, size etc)to enhance drug delivery.
13.00 Lunch
14.00 Physical form continued – salt selection and
survival in the GI tract, methods of analysis,
screening approaches
15.00 Tea
15.30 Consideration of changes in physical form and the
study of such changes. Underlying IP issues and
opportunities
16.30 An introduction to amorphous products for enhanced
drug delivery
17.30 Close
19.00 Course dinnerDay 2
9.00 Further discussion of solid dispersion
formulations
10.00 Solid lipid based options for drug delivery
11.00 Break
11.30 Solubilisation and cyclodextrin inclusion
complexes
12.30 Lunch
13.30 Practical approaches to selection of a formulation
route
14.30 Dissolution testing and consideration of food
effects etc
15.30 Tea
16.00 In vivo assessment of formulation strategies
17.00 Close of course
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Organized by:
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PharmaTraining Services |
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Invited Speakers:
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Prof Graham Buckton
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Deadline for Abstracts:
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N/A
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Registration:
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http://www.pharmatrainingservices.com/Challengesandformulationofinsolublecompounds2.htm
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E-mail:
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judy@pharmatrainingservices.com
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