We help biomedical and biotech companies protect their research IP, keep lab instruments and data systems running, and stay audit-ready for FDA and GxP requirements. From benchtop to cloud, your science stays secure and your environments stay validated.
Your proprietary formulations, sequences, and trial data are the entire value of the company, and they are a prime target for theft and industrial espionage. A single breach or insider leak can erase years of research and competitive advantage.
GxP and 21 CFR Part 11 require validated, documented, and controlled systems, but routine patching and IT changes can break validation if they are not managed carefully. Uncontrolled changes put your next audit and your data integrity at risk.
Sequencers, mass specs, and other instruments often run on aging or vendor-locked software that does not play well with modern security. Downtime or lost instrument data can stall experiments and ruin time-sensitive samples.
Long-running studies depend on years of accumulated data that cannot be recreated if it is lost or corrupted. Without tested backups and disaster recovery, a ransomware hit or hardware failure can wipe out irreplaceable work.
We harden your environment against IP theft and ransomware with security audits, MFA, email filtering, and continuous monitoring. Our work supports your GxP, 21 CFR Part 11, and SOC 2 readiness so you walk into audits prepared.
We design and run AWS, Azure, and GCP environments for research computing, LIMS, and data pipelines, with backups and disaster recovery built in. Validated cloud setups give you scale for genomics and analysis without losing control.
Our 24/7 helpdesk, endpoint monitoring, and controlled patch management keep lab workstations and instrument PCs secure without breaking validation. We document changes so your systems stay audit-ready and your researchers stay productive.
We lock down laptops, lab devices, and accounts with Zero Trust access and endpoint management so only the right people reach sensitive data. This limits insider risk and keeps IP from walking out the door.
Biomedical and biotech operations live under FDA oversight, GxP expectations (GLP, GMP, GCP), and 21 CFR Part 11 rules for electronic records and signatures. We help you maintain validated systems, audit trails, access controls, and documented change management so your data integrity holds up to inspection. If you handle clinical or patient data, we also support HIPAA safeguards and SOC 2 readiness alongside your quality processes.
Yes. We treat validated systems differently from general IT and follow documented, controlled change management for any patch or update. We coordinate with your quality team so changes are tested, recorded, and traceable, which keeps your audit trail and validation intact.
We layer defenses that include MFA, encrypted storage, email filtering, endpoint monitoring, and Zero Trust access so only authorized people reach sensitive research. We also monitor continuously and control device access to reduce both external attacks and insider risk. The goal is to keep your formulations, sequences, and trial data from leaving without permission.
Yes. Many instruments run on legacy or vendor-locked operating systems, so we isolate and protect those machines while keeping them functional. We segment them on the network, secure their data flows, and back up instrument output so an aging PC does not become a security hole or a single point of failure.
We set up backups and disaster recovery that are tested regularly, not just configured and forgotten. That means your long-running study data and instrument output can be restored to a known good state, so a ransomware event or failed drive does not erase years of work.