Life Sciences
Your science moves fast. Your systems have to prove it.
From the first lab buildout to an FDA inspection, centrexIT runs IT and security for life sciences companies as one team, so validation, data integrity and uptime are handled before anyone asks.
What we hear from organizations like yours
- Validation documentation lives in a binder, a spreadsheet, and someone's memory.
- Research data sits on instrument PCs and personal drives that nobody backs up.
- People paste data into AI tools faster than any policy can keep up.
- The company grew from a handful of scientists to a full team, and IT never caught up.
- When an instrument workstation fails mid-study, nobody knows how fast it comes back.
What changes when we run it
Validation you can show.
Systems documented for 21 CFR Part 11 and GxP as they are built, not the week before an audit.
Research data protected where it lives.
Backed up, access controlled, and recoverable.
AI use with guardrails.
Clear rules for which tools can touch which data.
One team for IT and security.
A person who answers and already knows your lab.
Why centrexIT
Biocom Endorsed Partner since 2017.
See Where You Stand
FDA Audit Readiness Score
Rate your 21 CFR Part 11 compliance readiness across electronic records and signatures.
Try Tool →Shadow AI Discovery
Find hidden AI tools across your organization. Identify risks before they find you.
Try Tool →HIPAA AI Decision Tree
Check your AI compliance requirements for healthcare with a guided decision framework.
Try Tool →Vendor Due Diligence Generator
Generate a comprehensive vendor security questionnaire for life science supply chain partners.
Try Tool →Request the conversation
You Call. We Answer. It Works.