Mission Statement
To promote the conduct of Quality Medical Research


The Success of our mission is dependent on using statistical methodology to:

- develop appropriate study designs,
- write statistical analysis plans,
- analyze data,
- create tables, listings, and graphs,
- write statistical sections for the medical literature or final reports.


The President of SSC, Inc. has over 20 years of experience in Biostatistics,
has co-authored over 50 articles in the medical journals, and co-authored a
book titled, "How to Report Statistics in Medicine"
which was translated into Chinese in 2002 and is currently in its 2nd Edition,
published by the American College of Physicians in 2006.



Click Here For President's Resume

     

P.O. Box 745
Chardon, Ohio 44024
Phone: 440-285-0735
Fax: 440-285-0849
consult@secicstats.com

 
statistical consulting services for clinical research which includes protocol design, sample size calculation, data analysis that support statistical design. Considerations on non-inferiority studies, equivalence studies should be taken on deciding your statistical strategy. Well written statistical section for clinical protocol is one statistical consulting service that Secic Statistical provides. Biostatistics statistical aspects of protocol development, statistics is the basis for your protocol. A Step-by-Step Approach to Non-Inferiority/Equivalency Trials Medical devices evolve incrementally. Non-inferiority or equivalency trials are often used to establish that a new device is the same as or no worse in performance than an existing device. This unusual strategy might be used to demonstrate that a material substitution in an existing device is undetectable by the customer, or it might be used to support a substantially equivalent argument in a 510k
.

[Next]

Web design by MSS Solutions Inc
Copyright © 2006 Secic Statistical Consulting Inc.
Last modified: 09/07/06
statistical report in medicine, statistical analyses in medicine, statistical section on protocol, statistical consulting in medicine, statistical consultant clinical research, protocol design, endpoints, sample size, equivalency studies statistical considerations,