#-supreme-cellcarta-differentiators-15-144{items-data:[{"text":"CAP-Accredited Sites "},{"text":"ISO Certified Standards"},{"text":"Global Execution "},{"text":"CLIA-Certified Labs "},{"text":"Clinical Preparedness "}]}#-supreme-cellcarta-faq-13-144{items-data:[{"faq_question":"What does CAP/CLIA accreditation mean for my study? ","faq_answer":"CAP/CLIA accreditations are internationally recognized quality credentials for clinical laboratories. For sponsors,it means CellCarta's laboratory processes,personnel qualifications,equipment,and test performance have been independently reviewed and meet the rigorous standards set by CAP/CLIA. Data generated in a CAP-accredited,CLIA-certified lab is widely accepted by regulatory agencies including the FDA and EMA. "},{"faq_question":"Which CellCarta laboratories hold CAP/CLIA certification? ","faq_answer":"

CellCarta maintains rigorous accreditation standards across its global network. All six of our labs —Antwerp (Belgium),Gosselies (Belgium),Jining (China),Lake Forest (USA),Montreal (Canada),and Naperville (USA) —hold CAP accreditation. Our sites in Antwerp (Belgium),Lake Forest (USA),Montreal (Canada),and Naperville (USA) additionally hold CLIA certificates of accreditation.

"},{"faq_question":"What ISO certifications do your laboratories hold? ","faq_answer":"

CellCarta has a global presence of ISO certified laboratories. The Antwerp clinical laboratory holds ISO 15189 and ISO 13485 certifications. The Naperville laboratory and logistics facility in Antwerp also hold ISO 13485 certification. ISO 27001 ISMS certification is maintained across all our global sites (Antwerp,Gosselies,Baulkham Hills,Jining,Montreal,Naperville) to protect clinical trial data and proprietary assay information.

"},{"faq_question":"How does CellCarta's QMS support regulated clinical trial testing? ","faq_answer":"CellCarta's QMS is implemented at all organizational levels under GCP,GLP,and GCLP regulations,covering study planning through data archiving. All processes are performed by qualified personnel and recorded in controlled documents including SOPs,Client Specific Procedures,and study worksheets that are approved prior to use. QA audits are performed by a dedicated Quality Assurance Unit to monitor performance and identify improvement opportunities. "}]}#-supreme-cellcarta-featured-resources-16-144{cards-data:[{"image_url":"\/wp-content\/uploads\/2026\/05\/webinar.jpg","card_type":"Webinar","date":"Feb 12","reading_time":"Reading Time - 5 minutes","title":"Resources Title Goes Here","description":"Lorem ipsum dolor sit amet,consectetuer adipiscing elit. Aenean commodo ligula eget dolor.","url":"#"},{"image_url":"\/wp-content\/uploads\/2026\/05\/webinar-2.jpg","card_type":"Webinar","date":"Feb 12","reading_time":"Reading Time - 5 minutes","title":"Resources Title Goes Here","description":"Lorem ipsum dolor sit amet,consectetuer adipiscing elit. Aenean commodo ligula eget dolor.","url":"#"},{"image_url":"\/wp-content\/uploads\/2026\/05\/webinar-3.jpg","card_type":"Webinar","date":"Feb 12","reading_time":"Reading Time - 5 minutes","title":"Resources Title Goes Here","description":"Lorem ipsum dolor sit amet,consectetuer adipiscing elit. Aenean commodo ligula eget dolor.","url":"#"}]}#-supreme-cellcarta-service-blocks-45-176{blocks-data:[{"image":"https://cellcarta.com/wp-content/uploads/2026/06/Capabilities-block-111.jpg","image_alt":"","title":"Biomarker Capabilities","description":"A full range of services across immune monitoring,proteomics,genomics,and histopathology. ","button_text":"Discover","button_url":"/capabilities/biomarkers/","button_target":"_self"},{"image":"https://cellcarta.com/wp-content/uploads/2026/06/Clinical-Trial-block-814.jpg","image_alt":"","title":"Clinical Trial Services","description":"Generate reliable, regulatory-ready data with harmonized global execution and integrated logistics.  ","button_text":"Discover","button_url":"/clinical-trial-services/","button_target":"_self"},{"image":"https://cellcarta.com/wp-content/uploads/2026/06/Data-Analytics-block-869.jpg","image_alt":"","title":"AI and Data Analytics ","description":"Analytical tools to break down complex datasets for key biological insights. ","button_text":"Discover","button_url":"/clinical-trial-services/ai-data-analytics/","button_target":"_self"}]}#-supreme-cellcarta-tab-content-11-144{tabs-data:[{"tab_title":"CAP/CLIA Accreditation ","content_title":"","content_body":"

Six CellCarta laboratories hold CAP and/or CLIA accreditation:

\n","tab_image":"https://cellcarta.com/wp-content/uploads/2026/07/CellCarta_-52-2-1-scaled.jpg","image_alt":""},{"tab_title":"ISO 15189/13485 ","content_title":"","content_body":"

The following facilities hold ISO 15189 (medical laboratory quality and competence) and/or ISO 13485 (quality management for medical devices) certification:

\n","tab_image":"https://cellcarta.com/wp-content/uploads/2026/06/ISO-tab-695.jpg","image_alt":""},{"tab_title":"ISO 27001","content_title":"","content_body":"

We have further ISO 27001 Information Security Management System (ISMS) certification across all our locations,including:

\n","tab_image":"https://cellcarta.com/wp-content/uploads/2026/06/ISO-27001-tab-831.jpg","image_alt":""},{"tab_title":"State-Specific ","content_title":"","content_body":"

CellCarta maintains state and regional clinical laboratory licenses and permits for sponsor programs requiring multi-state regulatory compliance.

\n","tab_image":"https://cellcarta.com/wp-content/uploads/2026/07/CellCarta_-41-2-scaled.jpg","image_alt":""},{"tab_title":"QMS ","content_title":"","content_body":"

Our global laboratories are maintained under one quality management system,driving harmonization of our testing sites and related activities.

\n

Read more about our QMS here.

","tab_image":"https://cellcarta.com/wp-content/uploads/2026/06/QMS-tab-885.jpg","image_alt":""}]}