|Quantity Discounts||1 - 9999|
|1 - 9999|
|1 - 9999|
Your company has invested millions in clinical trials. Now, a newly vigilant FDA has issued a final guidance that could put your hard-earned trial data at risk.
The ink is scarcely dry on a final guidance that requires you to tighten the monitoring of clinical trial investigators and subinvestigators — or pay the consequences.
The guidance includes an all-new section on Site Management Organizations (SMOs). Even people who’ve read it closely admit they may not grasp its full implications.
Wouldn’t it be great to spend 90 minutes with someone who does ... and who can interpret this tough new rule into plain English?
Industry pro Liz Wool is that person. She has read and analyzed the rule forward and backward — even marked it up and highlighted key sections. Now she’s sharing her hard-won knowledge with you.
FREE BONUS: You’ll also get a PDF copy of Ms. Wool’s own marked-up version of the final guidance, highlighting the key sections. You’ll want to share this crucial document with every person on your staff who shoulders clinical trial responsibilities.
Reserve time on Thursday, Dec. 17, for a 90-minute webinar with Ms. Wool as she covers these topics and more:
You’ll review case studies of past violations and how the new final guidance has been modified to compel compliance.
This webinar is totally interactive. You’ll get an opportunity to email your questions and receive answers by the time the session ends.
It’s the most economical way to educate dozens, even hundreds, of staffers and colleagues. Feel free to sign up as many registrants as you need to. There’s no limit as long as they’re at the same location.
Don’t delay — register NOW!
Liz Wool, RN, BSN, CCRA, CMT, is president and CEO of QD-Quality and Training Solutions Inc., a consulting firm offering SOPs, standards and training services to investigational site staff, sponsors and CROs. She has been active for 18 years in clinical research positions in sponsor companies, investigational sites, CROs and academia. She is president of the ACRP Northern California Chapter and teaches the CRA Certification Exam Review Course.
|Date:||Dec. 21, 2009 – Jan. 8, 2010|
|Location:||Your office or conference room (no need to travel!)|
Gather your team for maximum benefit! Your investment is for one dial-in.
We accept American Express, Visa and MasterCard. Make checks payable to FDAnews.
Or, register by phone: toll free (888) 838-5578 (inside the U.S.) or +1 (703) 538-7600
Registrations may not be cancelled. Please contact customer service to make any substitutions.
Interested in Becoming a Speaker?
We're always looking for industry leaders eager to share their expertise at an FDAnews audioconference, webinar or physical conference. Our seasoned speaker community includes executives in the pharmaceutical, medical device and clinical trial industries, regulatory affairs, quality control, compliance, healthcare and academia, as well as several former — and current — top FDA officials. Click here to complete our speaker opportunity form and have a representative contact you about future opportunities.
Copyright ©2018. All Rights Reserved. Design, CMS, Hosting & Web Development :: ePublishing