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Hands-on Tablet Development including principles of Pre-formulation, Formulation and Process Development (3 day)

Type Course
Language English
Date September 28, 2011 to
September 30, 2011
Venue County House, 221-241 Beckenham Road, Beckenham, BR3 4UF
221-241 Beckenham Road
Beckenham, Nr London BR3 4UF
GB
Chemistry Specialties
  • medicinal and pharmaceutical chemistry
Chemistry Techniques
  • other
Contact Judy Callanan
PharmaTraining Limited
BioCity, Pennyfoot Street
Nottingham, NG1 1GF
GB
44 (0) 115 9124249
44 (0) 207 6813582
judy@pharma-training-courses.com
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by Judy Callanan last modified 09-07-11 08:08 AM

This unique 3 day course is designed to integrate the key elements of tablet development with hands-on, practical experience in a small scale, lab scale test facility. Each day will consist of lectures on aspects of tablet development, followed by linked sessions in which participants take part in related experimental work. The course enables attendees to apply the theory learnt in the taught sessions, and also to directly observe the effect of formulation on product properties, and relate the theory to the practice of Quality by Design (QbD). Who Should Attend? • Newcomers to tablet formulation development and manufacturing • Production operators who need a better understanding of their products and how they have been developed • Analytical and QC staff who would benefit from understanding the tablet development and production process • Experienced personnel in one area of product development who need a broader overview • Project team members needing a broader insight into formulation development including preclinical, clinical, and project management representatives • Regulatory staff who would benefit from brief practical experience of the processes for which they are compiling dossiers. Regulatory agency staff requiring practical experience Numbers are restricted to 10 participants for maximum benefit Learning outcomes • Understanding of the relationship between Quality by Design, drug substance properties, formulation and process development • Practical experience of small scale tablet manufacture with direct knowledge of the relationship between formulation properties and tablet compressibility • Understanding of the roles of critical quality attributes, critical process parameters, and product control strategy in the application of the principles of QbD to formulation development

Speakers

Dr Michael Gamlen, Pharmaceutical Development Services has over 30 years experience of tablet development. Dr Dipankar Dey joined PharmaTraining Ltd from Oystar Manesty where he was Head of Process Development

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