Built for the regulated edges of healthcare and life sciences.
Same Kintavo platform, configured for the rules and rhythms of your domain. Browse by category — clinical operations, development & manufacturing, or specialized therapies.
Clinical operations & care delivery
Healthcare & Health Systems
Quality, accreditation, and incident programs that span hospitals, IDNs, and ambulatory networks — without the overhead.
Explore HealthcareClinical Laboratories
CLIA, CAP, and ISO 15189 quality programs purpose-built for clinical, anatomic path, and molecular laboratories.
Explore Clinical LabsBlood Banks & Transfusion
AABB, FDA, and ISBT-aligned workflows for blood banks, transfusion services, and apheresis programs.
Explore Blood BanksDevelopment, manufacturing & commercialization
Life Sciences
An umbrella platform for research, translational, and clinical-stage life-sciences organizations operating under GxP.
Explore Life SciencesPharma & Biotech
GMP-compliant quality for branded, generic, specialty pharma, and biologics — built for FDA, EMA, and PMDA scrutiny.
Explore Pharma & BiotechMedical Devices
ISO 13485 and 21 CFR Part 820 out of the box — with design controls, DHF management, and post-market surveillance.
Explore Medical DevicesCDMOs
Multi-client, multi-product quality systems for contract development & manufacturing — with sponsor-isolated data and reporting.
Explore CDMOsCROs
GCP-aligned quality and document control across multi-site, multi-sponsor clinical research operations.
Explore CROsSpecialized therapies & tissue programs
Cell & Gene Therapy
Patient-specific lots, chain-of-identity, and the regulatory rigor that comes with autologous and allogeneic therapies.
Explore Cell & GeneOrgan & Tissue
Tissue banks, transplant programs, and biorepository compliance — built for the chain of custody these programs demand.
Explore Organ & TissueDon't see your industry? Kintavo is configurable to any GxP-regulated environment. Talk to us about your specific compliance scope.
Talk to our team