Pharmaceutical Contract Research Organizations offer end-to-end support to the pharmaceutical, biotech, and medical device industries through services such as clinical trial management, regulatory submissions, data analysis, pharmacovigilance, and real-world evidence studies. By leveraging their scientific and regulatory expertise, CROs help reduce development time and cost while ensuring data accuracy and compliance. The Industry Iceberg CRO platform caters to a broad spectrum of segments, including
Industry Iceberg is an AI-enhanced global intelligence platform built for pharmaceutical, biotech, and life-science companies. It enables rapid identification of FDA‑compliant CROs, CMOs, analytical labs, pre‑clinical and clinical sites using 1.9 million data points across manufacturing, regulatory, and logistical parameters.
Thanks to 35+ filters and 42+ specification fields, your team can narrow down ideal facilities by compliance status, inspection history, certifications, location, capabilities, and more—enabling partner selection in under 30 seconds.
The platform covers an extensive range of facility types, including:
Absolutely! Industry Iceberg offers end‑to‑end oversight of facilities across continents, tracking readiness, capabilities, inspection status, and regulatory compliance across multiple agencies and jurisdictions through one unified dashboard.
We maintain trust by sourcing data from global regulatory authorities and audit sources. Our data is continuously verified, with AI/ML-powered analysis to ensure accuracy, relevance, and audit-readiness.
