New Audioconference: 'Are YOU Testing Unnecessarily?'
Some pharma/device manufacturers spend as much as three times more than others on test documentation.
Are they really getting three times the value?
Are YOU getting the most for YOUR testing dollar?
Get answers Tuesday, Nov. 25, in an audioconference for regulatory professionals sponsored by FDAnews. Register today!
Your presenter is G. Raymond Miller, Ph.D., of Miller Regulatory Consulting, a 25-year veteran of the computerization wars. His teams have performed more than 560 computer validation and 21 CFR 11 projects - with not a single 483 generated.
In just one hour on the phone, you'll discover - a.. The three UNNECESSARY test documentations that EVERYONE generates b.. The five bad habits that lead to excessive testing and documentation, and what YOUR company can do about them c.. How to save time, effort and $$$ by applying risk analysis to validation tasks and tests d.. How to manage test incidents and related documentation e.. Plus MUCH more! Sign up today if you are a - a.. Regulatory affairs professional b.. Information systems/information technology specialist c.. QA/QC expert d.. Validation team member Date: Tuesday, Nov. 25, 2003 Time: 1:30 p.m. - 2:30 p.m. EST Location: Your office Cost: $345 per dial-in
P.S. Participants save $150 on session CD and transcript! Click here. Audioconference, CD and transcript - pay only $540 CD and transcript - pay $345
To register: Phone: toll free (888) 838-5578 (inside the U.S.) or +1 (703) 538-7600 Web: http://www.fdanews.com/calendar/17035.html
Payment: Payment is required by the date of the audioconference. We accept the following credit cards: American Express, MasterCard and Visa.CONTACT:
300 N. Washington St., Suite 200
Falls Church, VA 22046-3431
Toll free: (inside US)(888) 838-5578
Main telephone: +1 (703) 538-7600
Fax: +1 (703) 538-7676
Posted: November 2003