TIDES 2010

Advancing Novel Therapeutics April 25 - 28, 2010 · Hynes Convention Center · Boston, MA

TIDES 2010

April 25 - 28, 2010 · Hynes Convention Center · Boston, MA

TIDES® continues to be the must-attend event for the industry as it grows in attendance each year.

Program highlights include:

  • CBER, FDA and 3 European regulatory agency speakers describe current expectations for quality and safety for approval of oligonucleotide and peptide therapeutics and vaccines
  • New dual tracks on CMC let you benchmark your company against industry leaders in manufacturing and analysis of API
  • Advances in formulation and delivery offer the latest updates for market expansion opportunities
  • Expanded break-out discussion sessions give you uncensored insights into the industry's most pressing challenges
  • Learn new skills and expand your knowledge with 5 cutting-edge pre-conference courses on the core disciplines of discovering, developing and manufacturing oligonucleotide and peptide-based therapeutics

Back by popular demand, expanded break-out discussion sessions and pre-conference courses give you the opportunity to gain behind-the-scenes insight into critical industry issues, and to ask your specific questions to the experts in a small group setting.

TIDES® is now the most comprehensive industry event with the addition of the 2nd Annual Oligonucleotide Therapeutics Discovery conference at the same venue

Co-Located Conferences
IBC's 6th International
Applications of Nucleic Acids Technologies in Molecular Diagnostics
Accelerating Product Development through Cutting Edge Regulatory,Business and Technology Strategies
IBC's 2nd Annual
Oligonucleotide Therapeutics Discovery
For Discovery, Preclinical and Early Development Scientists
April 27-28, 2010 April 26-28, 2010

Keynote Presentations

Elizabeth Mansfield, Ph.D.

Elizabeth Mansfield, Ph.D.
Director for Personalized Medicine, OIVD
CDRH, US FDA

William Pignato

William Pignato
Global Head, Regulatory Affairs
Novartis Molecular Diagnostics

  • Preclinical chemical modifications to improve drug-like properties
  • Overcoming cellular barriers to siRNA delivery
  • Nonclinical safety assessment strategies
  • 13 preclinical and clinical case studies
  • Techniques for oligo lead discovery and candidate selection
3-Day registration options provide access to all sessions and materials

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