Preclinical pharmaceutical services are vital in the early stages of drug development, ensuring that a drug candidate is safe and effective before entering clinical trials. These services include toxicology studies to evaluate potential toxicity through in vitro and in vivo tests, as well as pharmacokinetics (PK) and pharmacodynamics (PD) studies to understand how the drug is absorbed, distributed, metabolized, excreted, and its biological effects. Efficacy studies are conducted to assess the therapeutic potential of the drug in disease models, while bioanalytical services provide support for measuring drug levels and metabolites in biological samples. Additionally, regulatory support is offered to help prepare documentation and ensure compliance with regulatory guidelines.
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.
