Managing Risk for Clinical Trials
Tuesday, Sept. 9, 2014 • 1:30 p.m. - 3:00 p.m. EDT
Among the many issues that can derail a clinical trial, quality failures are surely the most frustrating.
Why? Because risk management techniques exist that can help you detect and mitigate the risks that can lead to clinical trial failures.
Those undetected flaws in your design and development process are preventable if, early in a trial, you incorporate risk management strategies such as Risk Management Plans and Quality by Design (QbD) tools.
The real question is: What are you waiting for?
On Sept. 9, the FDAnews webinar Managing Risk for Clinical Trials: Incorporating Quality by Design and Risk Management Strategies will help you make that critical choice.
With more than 50 years of combined experience, expert presenters Sherri Hubby and Brian Nugent will share insights that can be used to establish Risk Based Monitoring Plans, including triggers for return to 100% source data verification.
Even better, they'll show you how to proactively identify and manage risks to your trial with methods that can immediately be implemented and used.
You'll find out about QbD examples such as failure-modes-and-effects and criticality analysis (FMECA), Isikawa/Fishbone Diagrams, and Hazard Analysis and Critical Control Points (HACCPs).
And you'll learn these specifics:
BONUS: During the session, you'll also receive a copy of an invaluable risk assessment process/checklist to apply to your selection of vendors.
Attending Managing Risk for Clinical Trials: Incorporating Quality by Design and Risk Management Strategies might be the best decision you make in 2014.
After all, Risk Management Quality by Design (QbD) Strategies are encouraged by regulators such as the FDA and EMA. In fact, the QbD process was first introduced by the FDA — and is considered an important process and systematic approach to achieve clinical success.
Don't stop to think about it; register NOW.