Speed with control
Automate procurement from intake to assessment to contract, with guardrails that keep your policies in force.
ReportThe 2026 State of TPRMThe 2026 State of TPRM: where programs break and what risk leaders want insteadDownload
Biotech runs on CROs, CDMOs, and lab vendors. Coverbase shows who touches your data and IP, and how it's protected.
Your clinical and research partners hold your most valuable assets. Coverbase runs diligence and monitoring across every vendor in the GxP chain, without slowing the science.
CoverbaseBiotech | research partner
Biotech | research partner
A CRO's scope widens
Study protocol
Data access
Quality evidence
Agent work
01Compare the scope
02Review the evidence
03Assign the finding
Scope change ready for review
Quality and security decide together.
Why biotech teams choose Coverbase
- 01
GxP vendor oversight
Assess CROs, CDMOs, and lab partners against the quality and data-integrity standards your programs require. - 02
IP and data protection
Track which vendors touch research data and IP, and confirm the controls protecting them. - 03
Clinical trial vendor risk
Vet and monitor the vendors running trials, where a lapse can stall a program. - 04
Diligence that keeps up with R&D
Onboard new partners quickly so vendor risk doesn't hold up a milestone. - 05
Inspection-ready records
Keep complete documentation for in-scope vendors for audits and FDA inspections.
Vendor risk that respects the timeline
Programs move on hard deadlines. Coverbase makes diligence fast enough to keep up and thorough enough to defend.
Data-integrity focus
Assess vendors against the standards that keep clinical and lab data trustworthy.IP exposure mapped
See which partners hold sensitive research and how it's protected.Diligence prepared for your review
Evidence gathered and pre-reviewed automatically, so quality and security teams move faster.Audit-ready files
Pull a complete vendor record for inspections without a fire drill.
One platform for third-party risk and security
Explain with confidence
AI shows its reasoning for each recommendation, so you can explain your ratings, approvals, and exceptions.
Automate with assurance
Launch new workflows and adapt controls as your program and its regulations change.
How we protect your data
These are the practices behind the supplier records and evidence you keep in Coverbase. Read our security and privacy program.
To request our SOC 2 report or report a vulnerability, email security@coverbase.ai.
Independent review
A SOC 2 Type II audit against the AICPA Trust Services Criteria for security, availability, and confidentiality.Testing and remediation
External penetration tests every year, plus vulnerability scans and static and dynamic application security tests, with findings tracked through remediation.Identity and production access
SSO and SAML with Okta, Microsoft Entra, Google, and other identity providers. Multi-factor authentication is required for production access.Data protection
Data encrypted at rest with AES-256 and in transit with TLS 1.2 or higher.Internal accountability
Access logging, quarterly least-privilege reviews, and required employee security and privacy training.
Where does supplier diligence stop?
Your quality team owns validation; we track the partner review.
Can we apply our own GxP-related criteria?
Yes. We assess CROs, CDMOs, and labs against the controls your quality team sets for the activity. Your reviewers decide whether the evidence is sufficient.
Does Coverbase validate a clinical trial or a laboratory?
No. We organize supplier diligence and follow-up; we don't validate a clinical trial, laboratory, or quality system.
What happens when a partner's role expands?
We reopen the relationship record, check the new scope and evidence, and track any findings with an owner.