
Validation Services
Plan, execute, and document validation across LIS, EHR, instruments, and middleware. JTG helps laboratories meet regulatory requirements, ensure system accuracy, and support safe, reliable operations.
Validate new LIS, EHR, and instrument implementations
Support Operational Qualification testing with full documentation
Ensure compliance with CAP, CLIA, FDA, UKAS and AABB standards
Reduce risk during upgrades, integrations, and system changes
Deliver audit-ready validation without overloading your team
Our Services
Our team of clinical, laboratory, and technical experts partner with your team and vendors to plan, execute, and document validation across systems and workflows, supporting implementations, upgrades, integrations, and ongoing compliance requirements.
Transfusion and Donor
JTG provides comprehensive system validations performed according to regulatory and compliance standards. We cover all aspects of transfusion for blood bank and donor operations, including EHR/LIS communication, analyzers, as well as remote storage devices. Our clinical experience and comprehensive approach ensures patient safety and inspection readiness.
Instrumentation and Middleware
Whether you are implementing new instrumentation or middleware, or performing an upgrade; our validation services ensure quality assurance, quality control, calculations, and auto-verification parameters are meticulously defined and applied for each reportable test. We facilitate seamless integration to and from the LIS, ensuring all communication is accurate and reliable.
Project Management
Reach your project’s full potential with JTG’s project managers keeping lab initiatives on track from inception to go-live. Our project managers strategically allocate resources at the optimal times, ensuring timelines are met and costs are efficiently managed throughout the implementation process. With our expertise, milestones will be achieved, delays and added expenses avoided, and your team will stay focused on their goals.
JTG Experience
JTG supports validation across laboratory systems, including LIS, EHR, instrumentation, middleware, and transfusion environments. We work with labs to design test plans, execute validation scripts, and produce audit-ready documentation, ensuring systems perform as expected while maintaining compliance and patient safety.
Ascentry (BYG4lab)
Data Innovations
RALS
Roche Navify/infinity
Sysmex WAM & Caresphere
TELCOR
QuidelOrtho Results Manager
Beckman Coulter Remisol
Abbott AlinIQ
BD Synapsy
BD EpiCenter
And others
Abbott
BD
Beckman Coulter
BioFire
Bio-Rad
bioMérieux
Bruker
Cellavision
Cepheid
COPAN
Cytovale
DiaSorin
Dynex Technologies
Elektra
EliTech Group
GenMark Dx
Grifols
Haemonetics
Hologic
Illumina
Inflammatix
Luminex
PerkinElmer
Polymedco
Qiagen
PerkinElmer
Polymedco
Qiagen
QuidelOrtho
Radiometer
RALS
Roche
ROTEM
Sato
Sebia
Siemens
Stago
Starsed
Sysmex
Telcor
Tecan
Thermo Fisher
Varian
Ventana
Werfen
And others
Blood Bank Computer Systems (BBCS)
Cerner Millennium® & Cerner Bridge
Clinisys Blood Bank™ Management (Previously Sunquest Blood Bank™ Management)
El Dorado Donor
Epic BPAM
Gpi4Med.BLOOD
Haemonetics® SafeTrace Tx®, BloodTrack®, and BloodTrack Tx®
IT Synergistics bexWISE
MAK-Systems eProgesa®
MEDITECH
SCC SoftBank® and SoftDonor®
WellSky® Blood Centers (Previously Mediware LifeTrak)
WellSky® Transfusion (Previously Mediware HCLL)
Allscripts
Centricity
Cerner
eClinicalWorks
Epic
MEDITECH
OTTR
Picis
RALS
Remisol / SAP Crystal Reports
Sunrise Clinical Manager
Telcor
TouchWorks
WellSky
Xifin
bioMérieux
Bio-Rad Laboratories
Digi-Trax
eClinicalWorks
Grifols Diagnostic Solutions
Haemonetics
QuidelOrtho Clinical Diagnostics
Roche
Sato
Sysmex
Werfen
Successful Go-Lives
Structured validation planning and execution reduce risk during implementation, helping labs go live with confidence and fewer post-go-live issues.
Audit-Ready Documentation
Comprehensive validation documentation, including test results and risk assessments, ensures readiness for inspections and regulatory review.
Regulatory Compliance
Validation aligned with CAP, CLIA, FDA, UKAS and AABB standards ensures systems meet required guidelines and maintain compliance.
Accurate System Performance
Thorough testing across workflows, calculations, and interfaces ensures systems produce accurate and reliable results.
Reduced Operational Risk
Early identification of issues during validation prevents downstream errors, system failures, and workflow disruptions.
Improved Patient Safety
Validated systems support accurate testing, reporting, and data integrity, helping protect patient outcomes and clinical decisions.
Real Outcomes for
Lab Teams
Well-executed validation is required to ensure systems function correctly, meet regulatory requirements, and support safe, reliable laboratory operations. JTG takes on the heavy lift, reducing the burden on your team while ensuring nothing is missed.