Pharmaceutical services are crucial for the effective planning and execution of clinical trials, which are fundamental to the development and approval of new drugs. These services encompass comprehensive clinical trial management across all phases (I–IV), ensuring adherence to regulatory standards and protocols. Key components include patient recruitment and retention strategies, regulatory support for submissions to agencies like the FDA and EMA, and meticulous data management and analysis to maintain data accuracy and integrity. Additionally, biostatistical support is provided to interpret trial results, while pharmacovigilance ensures ongoing monitoring of drug safety. Clinical trial supply management also plays a vital role, handling the packaging, labeling, and distribution of study materials to ensure seamless trial execution. The Industry Iceberg Clinical 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.
