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Driving Innovation and Continuous Improvement in Pharmaceutical Analysis

• Assessing recent developments in separation sciences from collaborations with academia: Examples in high resolution/high speed LC, high
temperature LC and SFC
• Continuous improvement in a development environment.
• Determining tools and approaches for reducing overall cycle-times.

Jay Makwana, ARD Productivity, Innovation and External Collaborations Lead Associate Research Fellow, Pfizer Global R&D

 
Form Selection to Improve Solubility

• Screening and selection of the best form (polymorph, salt,cocrystal, amorphous, amorphous dispersion)
• Characterisation and performance assessment
• Development/formulation/processing issues to consider
• Phase I example for a poorly soluble compound

Dr Ann Newman, Vice President of Research and Development, Aptuit

 
Update on Patenting Solid Forms before the USPTO and EPO
Raymond Parker, Associate VP and Head , US Patent Operations, Internal Medicine Group, Sanofi-Aventis
 

Upcoming Events

  • Six Sigma in Pharma & Chemie
    Kundenwünsche qualitätsorientiert umsetzen – Prozesse effizient gestalten –Wettbewerbsfähig durch Lean Six Sigma Integration
    December 01 - 03, 2008 * Mövenpick Hotel, Berlin, Deutschland
  • 8th Annual Battlefield Healthcare
    Combat Casualty Care – From the Front Line to CONUS
    December 10 - 12, 2008 * Hilton San Antonio Airport, San Antonio, TX
  • Bio Banking 2009
    Optimizing Biospecimen Resources to Enable Biological Research
    January 12 - 15, 2009 * Philadelphia
  • Reducing Toxicity in Drug Compounds
    Reduce your failure rate in drug development by effective early stage toxicity modelling, prediction and testing
    January 26 - 27, 2009 * The Grosvenor Victoria, London, UK
  • Cool Chain Europe 2009
    January 27 - 29, 2009 * Sheraton Brussels Airport Hotel and Conference Centre, Brussels, Belgium
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