Laboratory development & accreditation
AC helps laboratories build the infrastructure, quality systems, and documentation needed to develop their diagnostic capability and achieve international and national accreditation.
For laboratories & hospitals
Advanced Consensus supports clinical laboratories in Jordan and the MENA region through two complementary service lines: building internal diagnostic capability — including accreditation under ISO 15189, CAP, and JFDA — and connecting to advanced genomic testing through internationally accredited reference partnerships for cases not yet within in-house scope.
AC helps laboratories build the infrastructure, quality systems, and documentation needed to develop their diagnostic capability and achieve international and national accreditation.
For tests outside current in-house capability, AC provides access to internationally accredited reference laboratories — keeping patient care complete while local capacity grows.
Lab development
AC works alongside laboratory teams to design or improve physical space, instrument placement, workflow sequencing, and pre-analytical processes — building a functional foundation before accreditation assessment begins.
AC guides laboratories through ISO 15189, CAP, and JFDA accreditation pathways — from initial gap assessment and documentation development through internal audit preparation and post-inspection follow-up.
AC helps laboratories identify which assays to develop in-house, which to validate, and which to access through reference partnerships — aligning the test menu to the laboratory's clinical context, equipment, and staff capability.
AC supports training programs and competency assessment frameworks appropriate to the laboratory's scope — covering analytical technique, quality system requirements, and accreditation documentation.
Accreditation
ISO 15189
International standard for medical laboratory quality and competence
The globally recognized framework for clinical laboratory quality management. AC supports laboratories through every phase — scope definition, quality manual development, method validation documentation, internal audit, and corrective action.
CAP
College of American Pathologists laboratory accreditation
One of the most recognized laboratory accreditation programs internationally. AC assists laboratories in understanding CAP checklist requirements, preparing inspection-ready documentation, and establishing ongoing compliance monitoring.
JFDA
Jordan Food and Drug Administration regulatory compliance
For laboratories operating under JFDA oversight, AC provides support in understanding applicable requirements, preparing regulatory submissions, and aligning quality systems with national standards.
Accreditation documentation, quality manual templates, and reference laboratory certificates are available to institutional partners. Specific documentation can be requested through the contact form.
Testing access
We review your institution's current send-out volume, target test categories, and operational requirements. No commitment required at this stage.
AC presents the relevant test categories, reference laboratory options, and logistics structure for your anticipated volume and use cases.
Ordering staff receive secure portal credentials. Requisition forms, specimen guides, and shipment instructions are provided for each test category.
AC reviews your sample collection and handling process to ensure specimens meet pre-analytical requirements — reducing avoidable rejection before cases are sent.
Initial cases are managed with direct AC support — from test selection and specimen review through to report delivery and clinical follow-up.
Once established, cases run through the agreed workflow. AC remains available for test queries, turnaround updates, and periodic menu reviews.
Get started
Suite 403, 133 Madina Munawara St, Amman, Jordan
+962 791 707 606 info@advancedconsensus.comMessage us on WhatsAppFor website inquiries, do not include patient names, medical record numbers (MRNs), national IDs, dates of birth, or identifiable reports or documents. Secure document exchange should happen through approved clinical channels.