Institute for International Research

Know how to achieve

Main menu

My IIR

Login form

Sign Up

Event Information

Registration

Online Registration is open!
Register Now!

Conference Brochure

Download Brochure
Full Event Details Inside

Customer Service

Have a question about this event?
Customer Service representatives are available to help from 8 AM - 6 PM EST
Call 888-670-8200

Need Technical Assistance With this Website?
Send an email to IIR's Web Department

Send To A Friend

Invite a colleague to join you at this event
Send to Friend

Add Event To Calendar

Save the event dates in your Outlook calendar
Add to Outlook Diary

Find another IIR Event

Event Search Form by Industry

Advanced Search

Formulation & Forced Degradation Strategies for Biomolecules

The only conference tying analytics into formulation
considerations and delivery techniques!

March 19 - 21, 2007 | Hilton San Diego Mission Valley, | San Diego, CA

Event Overview

Event Overview

Online Documentation Now Available!

Dear Analytical Scientists and Formulators:

Are you looking for more efficient ways to analyze and
characterize biomolecules for formulation and stability?

As an Analytical Scientist working on troubleshooting Stability-Indicating Assays, we encourage you to review these particular areas of the conference:

  • AM Workshop, March 19: Stability-Indicating Assay Development Methodology
  • PM Workshop, March 19: Analytical Strategies to Predict, Detect, and Control Extractables and Leachables
  • Track B, March 20: Design and Master Forced Degradation Strategies (featuring case studies and panel discussions)
  • Afternoon Plenary, March 20: Physical Characterization of PEGylated Peptides
  • Morning Plenary, March 21: Cutting-Edge High Throughput Analytical Testing Techniques
  • Track B, March 21: Orthogonal Methods for Degradant Analysis (featuring case studies and panel discussions)

As a Formulation Scientist working on troubleshooting Formulation Development & Delivery, we encourage you to review these particular areas of the conference:

  • AM Workshop, March 19: Stability-Indicating Assay Development to Predict Formulation Performance
  • PM Workshop March 19: Predict, Detect, and Control Extractables and Leachables- How will your delivery device effect this?
  • Track A, March 20: Phases & Stages- Key Formulation Approaches for Successful Development
  • Afternoon Plenary, March 20: Extrapolation of Results from Forced Degradation to Practical Formulation Development
  • Morning Plenary, March 21: Optimize Protein Formulation with the Use of Second Virial Coefficient Measurements
  • Track A, March 21: Drug Delivery and Formulation (featuring case studies and panel discussions)

FEATURED SPEAKERS

OPTIMIZING THE PROTEIN PURIFICATION PROCESS .

Prathima Acharya, PhD,
Sr. Scientist, Analytical & Formulation Development
DIOSYNTH BIOTECHNOLOGY


NEW TECHNOLOGIES!
.

Wm. Randy Forsyth, PhD,
Sr. Scientist, Emerging Sciences & Technology
TRANSFORM PHARMACEUTICALS




.Larry J. DeLucas, OD, PhD, DSc. (hon.),
Professor and Director of the Center for Biophysical Sciences and Engineering,
THE UNIVERSITY OF ALABAMA AT BIRMINGHAM
SPOTLIGHT ON AGGREGATION… .

Wei Wang, PhD,
Associate Research Fellow- Biologics,
PFIZER



FORMULATION DEVELOPMENT AND ANALYSIS….

Rob Simler, PhD,
Staff Scientist,
GENZYME CORPORATION


PROVIDING SOLUTIONS TO YOUR KEY ANALYTICAL &
FORMULATION CHALLENGES:

• Differences in Early vs. Late Stage Development
• Protein Aggregation
• Lyophilized Formulations
• Forced Degradation Testing
• Best Practice Degradant Analysis
• High Throughput Technology
• Drug Delivery
• PEGylated Proteins

 
INDIVIDUALIZE YOUR CONFERENCE LEARNING EXPERIENCE

- TWO New Workshops
- TWELVE + Case Studies
- FOUR Interactive Panel Discussions and
- FOUR Main Tracks

 


Click here to view our 2007
FFD Distinguished Speaking Faculty



Click here to view our 2007 Advisory Board.

TWELVE+ Case Studies:

  • Aggregation of Human Monoclonal Antibody during Formulation Development: A Structural Analysis by Vibrational Spectroscopy
  • Different Degradation Pathways in Liquid and Lyophilized Formulations
  • Challenges in the Development of a High Concentration Formulation
  • Confronting the Challenges of Formulation Development, Physical Characterization, and Analytical Evaluation of PEGylated Peptides
  • Structural Studies as a Screening Tool in Optimization of Protein Purification Processes
  • Selecting and Managing a Platform Technology Partner for the Sustained Released of Biomolecules
  • Generation, Identification, and Prevention of Aggregate Formation during Controlled Freeze-Thaw
  • Identify and Analyze Degradants using Mass Spectrometry
  • Investigating Potential Degradation Pathways of Recombinant Glycoproteins
  • Extrapolation of Results from Forced Degradation Studies to Practical Formulation Development
  • Strategies and Limitations of High Throughput Biomolecule Formulation Screening
  • Optimizing Protein Pharmaceutical Formulations with the Use of Second Virial Coefficients Measurements

Bottom menu

Copyright 2003-2006 IIR Holdings, Ltd. All rights Reserved

Powered by Interactive Agency Janmedia Interactive, Inc.