Why Sannova?


We will work with you on a personal level to provide you the most sensitive methods for your compounds, analyze your study samples and deliver incredibly accurate data within your tight timelines at competitive prices.


Over 250 validated BioA methods and hundreds of BioA projects completed and counting… Impeccable inspection record with the FDA as well as our sponsors.


Normally, it takes us only 3 to 4 weeks to: develop and validate an assay, analyze the samples and report the results.

Quality Results with Accountability!

90% of our ISR samples have a single digit %difference.

Facilitated NCE in the right direction and brought success to BE studies.

For every 1 scientist in our labs, we have 1 QC/QA person.

100% of all raw data is captured with our unique data-capture sheets, assuring you of our complete adherence to our SOPs.

Flexibility: 3 Business Models

1) We Provide BioA Services to you directly.

2) We’ll work hand-in-hand with your preferred clinical-provider.

3) We’ll provide Total Project Management Services from protocol design through final report submission in your preferred reporting format.

All Sannovians have PASSION and OWNERSHIP of the work we do for YOU.