{"id":11,"date":"2026-03-14T15:49:57","date_gmt":"2026-03-14T15:49:57","guid":{"rendered":"https:\/\/3edia.ca\/icts\/services\/"},"modified":"2026-03-14T15:49:57","modified_gmt":"2026-03-14T15:49:57","slug":"services","status":"publish","type":"page","link":"https:\/\/3edia.ca\/icts\/services\/","title":{"rendered":"Services"},"content":{"rendered":"<style>@import url('https:\/\/fonts.googleapis.com\/css2?family=DM+Sans:wght@300;400;500;600;700;800;900&display=swap');<\/style>\n<section style=\"background:linear-gradient(135deg,#0A1C4F 0%,#1B5DED 100%);padding:120px 40px 80px;font-family:'DM Sans',sans-serif;text-align:center;\">\n<div style=\"max-width:800px;margin:0 auto;\">\n    <span style=\"display:inline-block;background:rgba(255,255,255,0.15);color:rgba(255,255,255,0.9);font-size:12px;font-weight:700;letter-spacing:2px;text-transform:uppercase;padding:8px 20px;border-radius:50px;margin-bottom:24px;\">Our Services<\/span><\/p>\n<h1 style=\"font-family:'DM Sans',sans-serif;font-size:clamp(36px,5vw,58px);font-weight:800;color:#fff;margin:0 0 24px;letter-spacing:-1px;\">End-to-End Clinical Trial Management<\/h1>\n<p style=\"font-size:18px;color:rgba(255,255,255,0.8);line-height:1.7;max-width:600px;margin:0 auto;\">From site selection to data management \u2014 iCTS handles every phase of the clinical trial process with precision, integrity, and empathy.<\/p>\n<\/p><\/div>\n<\/section>\n<section style=\"background:#f8f9fc;padding:100px 40px;font-family:'DM Sans',sans-serif;\">\n<div style=\"max-width:1200px;margin:0 auto;\">\n<div style=\"display:grid;grid-template-columns:repeat(3,1fr);gap:32px;\">\n<div style=\"background:#fff;border-radius:16px;padding:36px 32px;box-shadow:0 2px 20px rgba(10,28,79,0.07);border:1px solid rgba(10,28,79,0.06);\">\n<div style=\"width:52px;height:52px;background:#EEF3FD;border-radius:12px;display:flex;align-items:center;justify-content:center;margin-bottom:24px;font-size:24px;\">\ud83d\udd2c<\/div>\n<h3 style=\"font-family:'DM Sans',sans-serif;font-size:18px;font-weight:700;color:#0A1C4F;margin:0 0 12px;\">Site Selection &#038; Investigator Selection<\/h3>\n<p style=\"font-size:15px;color:#666;line-height:1.7;margin:0;\">Strategic identification and qualification of optimal trial sites and principal investigators across the US and West Africa.<\/p>\n<\/p><\/div>\n<div style=\"background:#fff;border-radius:16px;padding:36px 32px;box-shadow:0 2px 20px rgba(10,28,79,0.07);border:1px solid rgba(10,28,79,0.06);\">\n<div style=\"width:52px;height:52px;background:#EEF3FD;border-radius:12px;display:flex;align-items:center;justify-content:center;margin-bottom:24px;font-size:24px;\">\ud83d\udccb<\/div>\n<h3 style=\"font-family:'DM Sans',sans-serif;font-size:18px;font-weight:700;color:#0A1C4F;margin:0 0 12px;\">IRB, Ethics &#038; DSMB<\/h3>\n<p style=\"font-size:15px;color:#666;line-height:1.7;margin:0;\">Comprehensive IRB, Ethics Committee, and Data Safety Monitoring Board consultation, review and submission management.<\/p>\n<\/p><\/div>\n<div style=\"background:#fff;border-radius:16px;padding:36px 32px;box-shadow:0 2px 20px rgba(10,28,79,0.07);border:1px solid rgba(10,28,79,0.06);\">\n<div style=\"width:52px;height:52px;background:#EEF3FD;border-radius:12px;display:flex;align-items:center;justify-content:center;margin-bottom:24px;font-size:24px;\">\ud83d\udc65<\/div>\n<h3 style=\"font-family:'DM Sans',sans-serif;font-size:18px;font-weight:700;color:#0A1C4F;margin:0 0 12px;\">Patient Enrolment<\/h3>\n<p style=\"font-size:15px;color:#666;line-height:1.7;margin:0;\">Community-anchored patient recruitment strategies ensuring diverse, representative participation in clinical trials.<\/p>\n<\/p><\/div>\n<div style=\"background:#fff;border-radius:16px;padding:36px 32px;box-shadow:0 2px 20px rgba(10,28,79,0.07);border:1px solid rgba(10,28,79,0.06);\">\n<div style=\"width:52px;height:52px;background:#EEF3FD;border-radius:12px;display:flex;align-items:center;justify-content:center;margin-bottom:24px;font-size:24px;\">\ud83d\udcca<\/div>\n<h3 style=\"font-family:'DM Sans',sans-serif;font-size:18px;font-weight:700;color:#0A1C4F;margin:0 0 12px;\">Data Management<\/h3>\n<p style=\"font-size:15px;color:#666;line-height:1.7;margin:0;\">Rigorous data collection, management and analysis ensuring integrity, accuracy, and full regulatory compliance.<\/p>\n<\/p><\/div>\n<div style=\"background:#fff;border-radius:16px;padding:36px 32px;box-shadow:0 2px 20px rgba(10,28,79,0.07);border:1px solid rgba(10,28,79,0.06);\">\n<div style=\"width:52px;height:52px;background:#EEF3FD;border-radius:12px;display:flex;align-items:center;justify-content:center;margin-bottom:24px;font-size:24px;\">\ud83c\udfe5<\/div>\n<h3 style=\"font-family:'DM Sans',sans-serif;font-size:18px;font-weight:700;color:#0A1C4F;margin:0 0 12px;\">Clinical Monitoring<\/h3>\n<p style=\"font-size:15px;color:#666;line-height:1.7;margin:0;\">On-site and remote monitoring services ensuring protocol compliance and patient safety throughout the trial.<\/p>\n<\/p><\/div>\n<div style=\"background:#fff;border-radius:16px;padding:36px 32px;box-shadow:0 2px 20px rgba(10,28,79,0.07);border:1px solid rgba(10,28,79,0.06);\">\n<div style=\"width:52px;height:52px;background:#EEF3FD;border-radius:12px;display:flex;align-items:center;justify-content:center;margin-bottom:24px;font-size:24px;\">\ud83d\udcdd<\/div>\n<h3 style=\"font-family:'DM Sans',sans-serif;font-size:18px;font-weight:700;color:#0A1C4F;margin:0 0 12px;\">Regulatory Affairs<\/h3>\n<p style=\"font-size:15px;color:#666;line-height:1.7;margin:0;\">End-to-end regulatory strategy and submission support for IND applications, protocol amendments, and safety reporting.<\/p>\n<\/p><\/div>\n<div style=\"background:#fff;border-radius:16px;padding:36px 32px;box-shadow:0 2px 20px rgba(10,28,79,0.07);border:1px solid rgba(10,28,79,0.06);\">\n<div style=\"width:52px;height:52px;background:#EEF3FD;border-radius:12px;display:flex;align-items:center;justify-content:center;margin-bottom:24px;font-size:24px;\">\ud83c\udf0d<\/div>\n<h3 style=\"font-family:'DM Sans',sans-serif;font-size:18px;font-weight:700;color:#0A1C4F;margin:0 0 12px;\">Grant Programs<\/h3>\n<p style=\"font-size:15px;color:#666;line-height:1.7;margin:0;\">Service grant programs designed to support investigators and institutions seeking to advance clinical research capacity.<\/p>\n<\/p><\/div>\n<div style=\"background:#fff;border-radius:16px;padding:36px 32px;box-shadow:0 2px 20px rgba(10,28,79,0.07);border:1px solid rgba(10,28,79,0.06);\">\n<div style=\"width:52px;height:52px;background:#EEF3FD;border-radius:12px;display:flex;align-items:center;justify-content:center;margin-bottom:24px;font-size:24px;\">\ud83e\udd1d<\/div>\n<h3 style=\"font-family:'DM Sans',sans-serif;font-size:18px;font-weight:700;color:#0A1C4F;margin:0 0 12px;\">Community Outreach<\/h3>\n<p style=\"font-size:15px;color:#666;line-height:1.7;margin:0;\">Deep community engagement strategies to build trust and ensure sustainable, diverse patient recruitment pipelines.<\/p>\n<\/p><\/div>\n<div style=\"background:#fff;border-radius:16px;padding:36px 32px;box-shadow:0 2px 20px rgba(10,28,79,0.07);border:1px solid rgba(10,28,79,0.06);\">\n<div style=\"width:52px;height:52px;background:#EEF3FD;border-radius:12px;display:flex;align-items:center;justify-content:center;margin-bottom:24px;font-size:24px;\">\u2695\ufe0f<\/div>\n<h3 style=\"font-family:'DM Sans',sans-serif;font-size:18px;font-weight:700;color:#0A1C4F;margin:0 0 12px;\">Scientific Advisory<\/h3>\n<p style=\"font-size:15px;color:#666;line-height:1.7;margin:0;\">Access to our distinguished Scientific Advisory Board for guidance on study design, endpoints and scientific integrity.<\/p>\n<\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/section>\n<section style=\"background:linear-gradient(135deg,#1B5DED,#16B4EE);padding:80px 40px;font-family:'DM Sans',sans-serif;text-align:center;\">\n<div style=\"max-width:700px;margin:0 auto;\">\n<h2 style=\"font-family:'DM Sans',sans-serif;font-size:40px;font-weight:800;color:#fff;margin:0 0 20px;\">Ready to get started?<\/h2>\n<p style=\"font-size:18px;color:rgba(255,255,255,0.85);margin:0 0 40px;line-height:1.7;\">Partner with iCTS for your next clinical trial. We bring expertise, community, and integrity to every engagement.<\/p>\n<p>    <a href=\"\/icts\/contact-us\" style=\"display:inline-flex;align-items:center;gap:10px;background:#fff;color:#1B5DED;font-family:'DM Sans',sans-serif;font-weight:700;font-size:16px;padding:18px 40px;border-radius:8px;text-decoration:none;\">Contact Us Today \u2192<\/a>\n  <\/div>\n<\/section>\n","protected":false},"excerpt":{"rendered":"<p>Our Services End-to-End Clinical Trial Management From site selection to data management \u2014 iCTS handles every phase of the clinical trial process with precision, integrity, and empathy. \ud83d\udd2c Site Selection &#038; Investigator Selection Strategic identification and qualification of optimal trial sites and principal investigators across the US and West Africa. \ud83d\udccb IRB, Ethics &#038; DSMB [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-11","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/3edia.ca\/icts\/wp-json\/wp\/v2\/pages\/11","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/3edia.ca\/icts\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/3edia.ca\/icts\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/3edia.ca\/icts\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/3edia.ca\/icts\/wp-json\/wp\/v2\/comments?post=11"}],"version-history":[{"count":0,"href":"https:\/\/3edia.ca\/icts\/wp-json\/wp\/v2\/pages\/11\/revisions"}],"wp:attachment":[{"href":"https:\/\/3edia.ca\/icts\/wp-json\/wp\/v2\/media?parent=11"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}