CDISC – ZBI Expertise
No other company can offer ZBI’s combination of CDISC experience and expertise.
We’re active and leading members of the CDISC and HL7 standards-writing teams. Look at our extensive track record of training programs and seminars
to see the extraordinary range of topics we cover and the exceptional
breadth of government agencies and pharma, biotech, and information
companies we’ve served.
Case 1: Our client needs everything, now.
They challenged
ZBI to bring their entire data management, analysis, and programming
shop, including managers, up to speed on CDISC submission standards so
that urgent client needs can be met and exceeded.
The ZBI Solution:
Our off-the-shelf, on-site, and very economical one-day CDISC training
program, including customization for client's own data practices.
Case 2: Major Pharma seeks strategic guidance on CDISC and HL7.
They asked us to perform a strategic overview of CDISC and HL7
standards to help guide their clinical data initiative planning and to
give their U.S. and European-based staff the same view of the clinical
data future.
The ZBI Solution:
A custom three-day program, tailored to management in the first
half-day and segmented for other specialties during days two and three,
drawing from the client's own work and including hands-on workshops.
Case 3: FDA deadline nears, database isn’t ready.
Our client asked us to provide the consulting and software tools to
enable the near-term submission of a state-of-the-art CDISC clinical
database to FDA.
The ZBI Solution:
We analyzed the client's data stream and recommended where and how to
transform it, deploying CDISC's proprietary Tekoa Technology to
custom-generate XML define documents for submission to the FDA.
There’s a CDISC solution for you, and we have it. Call 973-727-0025 today or e-mail ZBI today to learn more.
