1. Decrease your OOS problems and improve the precision of your assay by hearing the latest approaches to tame your noisy data from a statistical, biological and regulatory perspective
2. Practical truths about selecting and maintaining reference material which will keep you out of regulatory hot water; statistical plans, tracking and trending protocols and case studies
3. Avoid the pitfalls in your programs and hear the truth about the trials and triumphs of implementing USP recommendations for assessing similarity
4. Learn the tricks of the trade to run an efficient and compliant bioassay QC laboratory
5. Hear new trends & case studies about developing, qualifying and validating complex bioassays from your colleagues in bioassay development
Find out more about this year’s program by downloading the agenda.
If you’d like to join us May 5-7, 2014 in Berkeley, California, as a reader of this blog, you’re eligible for 20% off the standard rate when you register to join us and mention code B14177JT. Have any questions or want to get involved? Feel free to reach out to me at jpereira@iirusa.com.
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