Feuerbach and Associates

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Clinical Trial and Scientific Data Analysis Consultants
to the Biotechnology and Pharmaceutical Industries

We are experts in preparing, analyzing, reporting and validating laboratory, cardiac, endocrine, oncology, anti-viral and analgesic drug study data.

Services Provided:

SAS programming.
Data Visualization/Patient Profile systems.
Electronic regulatory submissions using CDISC standards and CRT/SDTM data files.
Design of reuseable, standardized code using the SAS/Macro facility.
Evaluation, configuration and setup of your datacenter hardware and software.
Creation of data marts for data mining.
Analysis of clinical trial, pharmacokinetic, epidemiological and product stability data using SAS statistical analysis software.
U.S. FDA and International regulatory submissions for new drug applications.
Development of integrated data analysis systems for the pharmaceutical and biotechnology industries.
Design of complex graphical reporting software with SAS/GRAPH.
Validation of applications software and data to 21 CFR Part 11 requirements.
Creation of user friendly interfaces with SAS/FSP and SAS/AF.
Extensive use of the SAS macro facility to provide reusable software.
UNIX system administration.
Clinical Data Management.
Web Design.

Let Feuerbach & Associates show you how they can provide for your clinical and scientific data analysis needs.

If you have comments, questions or need a consulting SAS programmer, email

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