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FIP/SIG Workshop: Special dosage forms – What’s new with in vitro drug release?

 
  May 22, 2008

Pharmacology and Toxicology

 
     
 
Royal Pharmaceutical Society of Great Britain, London
Monday 20-Tuesday 21 October 2008


Monday 20 October

Keynote Presentations         
13:00 – 13:10  Introduction and Welcome  
Vinod P. Shah, FIP, BPS, USA 
13:10 – 13:50  Current views of European Pharmacopeia on the Drug Release of Special Dosage Forms
Susanne Keitel, EDQM, Germany 
13:50 – 14:30   Overview of USP Dosage Form Taxonomy
Todd Cecil, USP, USA 
14:30 – 15:10   Overview of Current FIP SDF White Paper
Jennifer Dressman, University of Frankfurt, Germany
15:10 – 15:30  Coffee Break 

Session 1: Specialized Oral Dosage Forms
Moderators: Jennifer Dressman, University of Frankfurt, Germany and Cynthia Brown, Eli Lilly & Compnay, USA

15:30 – 16:10 Orally Disintegrating Tablets – Disintegration vs Dissolution Lucinda Buhse, FDA, USA 
16:10 – 16:50 Buccal Dosage Forms
Munir Hussain, Bristol Meyer Squibb, USA 
16:50 – 17:30 Chewable Oral Drug Products
J ohannes Kraemer, PHAST, Germany
17:30 – 18:00  Panel Discussion 

Tuesday 21 October
Session 2:  Non-Oral Dosage Forms

Moderators: Johannes Kraemer, PHAST, Germany and Mary Stickelmeyer, Eli Lilly & Company, USA
 
08:00 – 08:10 Welcome – Session Overview
 
08:10 – 08:50 Topical
Clarence Ueda, University of Nebraska, USA 
08:50 - 09:30  Opthalmics
Larry Stevens, Alcon Research, USA
09:30 -10:00  Break 
10:00 – 10:40 Drug-eluting Stents - Industry Perspective
Lori Allgeuier, Cordis, USA     
10:40 – 11:20 Drug-eluting Stents  - Regulatory Perspective
Angelica Durantes, FDA , USA
11:20 – 12:00  Panel Discussion
12:00 – 13:00  Lunch 

Session 3: Special Dosage Forms
Moderators: Mike Morris, Irish Medicines Board, Ireland and Todd Cecil, United States Pharmacopeia, USA 
13:00 – 13:40 Microspheres
Siddhesh Patil, Amylin, USA 
13:40 – 14:20 Nanoparticles
Roy De Maesshlack, Johnson & Johnson, Belgium
14:20 – 15:00 Liposomes Dr Hiroshi Kikuchi, Eisai Co.,Japan 
15:00 – 15:30 Break  
15:30 – 16:10
Is It Time for In Vitro Release Testing of Inhalation Dosage Forms?
Neal Davies, University of Washington, USA 
16:10 – 16:40 In vitro release of suppositories
TBC
16:40 – 17:20 Panel Discussion 
17:20 – 17:30 Conclusions and next steps

 

 
 
Organized by: Royal Pharmaceutical Society of Great Britain
Invited Speakers: Horst-Dieter Friedel, Bayer HealthCare AG, GermanyCynthia K. Brown, Eli Lilly & Company, USAVinod P. Shah, FIP Scientific Secretary, USALucinda Buhse, Food and Drug Administration (FDA), USASusanne Kietel, European Directorate for the Quality of Medicines and Healthcare, GermanyMary Stickelmeyer, Eli Lilly & Company, USAJohannes Kraemer, PHAST, GermanyTodd Cecil, United States Pharmacopeia, USAMike Morris, Irish Medicines Board, Ireland
 
Deadline for Abstracts: N/a
 
Registration:

12.15

E-mail: science@rpsgb.org
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