10 datasets found
Directory of research institutions and medical centers actively conducting FDA-regulated psilocybin-assisted therapy clinical trials, covering treatment-resistant depression, MDD, addiction, and other psychiatric indications across North America and Europe.
Directory of biobank storage providers offering GLP, GCLP, and GMP-compliant specimen storage for clinical trials, translational research, and long-term biorepository management across global facilities.
A curated database of biotech companies with gene therapies in active clinical trials, covering AAV, lentiviral, and CRISPR-based platforms across rare disease, oncology, and cardiovascular indications. Built for biotech investors, pharma BD teams, and clinical supply chain vendors evaluating partnership or acquisition targets.
Comprehensive directory of FDA/CE-cleared wearable biosensor manufacturers building clinical-grade devices for remote patient monitoring, decentralized clinical trials, and continuous vital sign tracking.
A curated database of medical institutions conducting FDA-registered stem cell clinical trials across the United States, including trial phases, therapeutic areas, and principal investigators — helping referring physicians and researchers identify legitimate programs.
Comprehensive database of AI-driven platforms that match patients to clinical trials using NLP, real-world data, and EHR mining. Ideal for clinical operations teams evaluating technology partners to accelerate patient recruitment and enrollment.
Comprehensive directory of EDC software vendors for clinical trials, including platform capabilities, regulatory compliance status, and deployment models. Built for clinical operations teams evaluating data capture solutions that meet 21 CFR Part 11 requirements.
Comprehensive database of contract research organizations specializing in oncology clinical trials, including therapeutic focus areas, trial phase capabilities, global site networks, and regulatory track records for CRO selection and vendor qualification.
Comprehensive database of CROs specializing in medical device clinical trials, covering 510(k), PMA, and De Novo pathways with biocompatibility testing, usability studies, and regulatory submission support.
Comprehensive database of CROs specializing in Phase 1 and first-in-human clinical trials, including bed capacity, therapeutic focus, regulatory jurisdictions, and global site locations for biotech sponsors outsourcing early-phase development.