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About Sigma-Chi
For more than a decade, Sigma-Chi has helped pharmaceutical and biotech sponsors turn clinical data into accurate, submission-ready results, with teams in the USA, Germany and India.
Home / About Us
For more than a decade, Sigma-Chi has helped pharmaceutical and biotech sponsors turn clinical data into accurate, submission-ready results, with teams in the USA, Germany and India.
Sigma-Chi was founded with a simple idea: sponsors deserve a biometrics partner that combines deep statistical expertise with dependable, on-time delivery. Today our statisticians, programmers and data managers support studies from protocol design through regulatory submission.
We work as an extension of your team, with a dedicated point of contact, transparent communication and audit-ready documentation, so you always know where your study stands.
Statisticians and programmers who have seen it all.
Clear plans and no surprises at database lock.
Across phases, indications and submission types.
The same experts from first study to last.
Long-term partnerships with CROs and biotechs.
Audit-trail documentation built into every output.
Innovative methodologies and experienced teamwork maintain the highest quality, with on-time deliverables for each clinical study. This is the biggest strength of our company.
Sigma-Chiconsulting offers a complete menu of biostatistical and programming services. Sponsor companies can choose the services that meet their needs, from assisting with protocol development to statistical analysis and reporting by our biostatisticians.
To turn clinical data into reliable, submission-ready evidence, on time and right the first time.
We combine expert biostatisticians, programmers and data managers with smart automation, so sponsors can make confident decisions and bring new therapies to patients sooner.
To be the most trusted biometrics and AI-enabled clinical data partner for pharma and biotech worldwide.
We see a future where every study is reported faster, with fewer errors, through teams and tools that set the standard for quality in clinical research.
Independent double programming, documented QC and AI-assisted checks on every deliverable.
Clear plans, realistic timelines and proactive updates, with no surprises at database lock.
One point of contact and a team that learns your standards and stays with your program.
We invest in automation and AI, like our TLF QC tool, to make clinical reporting faster and cleaner.
Delivery across US, European and Indian time zones keeps work moving every day.
SDTM, ADaM, Define-XML and TLFs built to current standards in SAS and R.
Our AI TLF QC tool catches layout, shell and consistency issues before manual review.
Teams in Hyderabad and Visakhapatnam with backup coverage for critical roles.
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