Posted: 7-Apr-2008
** New Live Online Course **
Best Practices in SAS Statistical Programming for Regulatory
Submission
These courses are intended for anyone directly or indirectly
responsible for the creation, content or validation of
summary tables, data lists and graphs used to support
research, drug or medical device efficacy and safety in a
regulatory submission. Professionals in the pharmaceutical,
biotechnology and medical device industries who want to be
21 CFR Part 11 compliant with effective and practical
solutions to address real-world issues will benefit from
these unique courses.
- Next live online class, May 20, 2008
at 11:00 a.m. - 12:30 p.m. (EST New York time):
Best Practices in SAS Statistical Programming for
Regulatory Submission: Creating Publication-Quality
Summary Tables (SECOND online course in a Two-Part
Series) Limited seats, register now!
http://www.cfpa.com/200805202214-15a/2214/t/2214/0/CourseSearch.aspx
Please see this link for more information:
http://www.sascommunity.org/wiki/Best_Practices_in_SAS_Statistical_Programming_for_Regulatory_Submission |
