Life Sciences IT

Validated, audit-ready IT for research, clinical, and manufacturing

We deliver managed IT and cybersecurity for biotech, pharma, medical device makers, and CROs - with 21 CFR Part 11 validation, lab-instrument support, and IP protection that stands up to FDA and partner scrutiny.

[ STATUS ]
24/7 SOC

Active Monitoring

Live threat intel · less than an hour response SLA · US-based senior engineers.

[ CALL ]
864-224-0008

Support · 24/7

Dial
[ 01 ]
Part 11
Validated systems inventory
[ 02 ]
100%
Lab instruments segmented
[ 03 ]
Audit-ready
Sponsor / FDA evidence packages
[ 04 ]
24/7
Research & clinical SOC
Why teams switch

The pressure on Life Sciences IT keeps rising

We've spent years inside life sciences environments. These are the patterns we see - and what we do about them.

FDA inspections don't wait

21 CFR Part 11 audit trails, e-signatures, and validated systems have to hold up under 483 scrutiny.

Lab instruments are on your network

HPLCs, mass specs, sequencers, and imaging systems run legacy OSes and rarely get patched.

Research IP is your valuation

A breach of research data, formulations, or clinical data can move enterprise value materially.

Sponsors and partners audit you

Big pharma sponsors, VCs, and acquirers now audit CROs and biotech IT before signing.

What you get with us

  • 21 CFR Part 11 / GxP
  • Lab instrument networks
  • Research IP protection
  • Clinical trial data integrity
What we deliver

A complete Life Sciences IT and security program

Not a menu of disconnected tools - one accountable team running it end to end.

21 CFR Part 11 / GxP program

System inventory, validation packages (IQ/OQ/PQ), audit trails, e-signature controls, and change management.

Lab instrument networks

Segmented instrument VLANs, vendor-aware patching, and monitoring for HPLC, MS, NGS, and imaging systems.

Research IP protection

Data classification, DLP, ELN / LIMS access governance, and offboarding for departing researchers.

Clinical trial data integrity

ALCOA+ controls, EDC platform support, and backups tuned for clinical data retention.

Sponsor & partner audit support

Evidence packages and interviews for sponsor, VC, and acquirer IT and security audits.

Compliance

The frameworks we map to

We build to recognized frameworks so your regulators, customers, and board see the work.

21 CFR Part 11GxP (GLP / GCP / GMP)HIPAA (clinical data)EU Annex 11ISO 27001SOC 2 (for sponsors)
FAQ

Life Sciences IT - common questions

Get started

Ready for Life Sciences IT that just works?

Book a 30-minute call. We'll review your environment and tell you, honestly, what to fix first.