In this session, seasoned industry experts:
- explore how to effectively set up your pre-clinical POC studies
- address pre-clinical safety requirements and issues
- give you an overview of the manufacturing standards required for Phase I studies
At the end of the session, you have a better understanding of the IND requirements as well as how to ensure that your studies provide adequate information for you to make informed decisions on the the design of your first clinical study.
SPEAKERS
Wendy Hill -Gap Strategies
Valentia Lee Brotherton - Ashuren
Peter Pekos - Dalton Pharma
DATE | TIME | LOCATION
May 13, 2008
5:00PM - 7:00PM
MaRS Centre, CR-2
101 College St.
Toronto, ON
MORE INFORMATION
For more information about this event, please email our Events Coordinator at:
events@marsdd.com 416-673-8100
Click here for more information about the Best Practices Event Series >>
WEBCAST

Click to watch the webcast and download the presentation
| |
PRESENTATIONS
- Optimizing Preclinical Proof of Concept
- Preclinical Development Planning for Emerging Pharma and Biotech Firms
- Preparing an IND Application: CMC
- Best Practices: From Benchtop to IND
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