Cato Research is an international regulatory & clinical contract research organization that has been delivering successful outcomes for its clients for 30 years. Through highly qualified & experienced personnel located in offices across North America, Europe, Israel, & South Africa, supported by strategic alliances with selected regional CROs, CATO offers tried & trusted international coverage. CATO has the advantage of integrated regulatory, clinical, & scientific expertise. Our highly talented & experienced international team offers services from preclinical through IND (or equivalent), clinical development, & marketing approval to Phase 4 postmarketing research. Our track record includes successes across many different health products, including drugs, biologics, vaccines, cell therapies (including stem cells), nutriceuticals, medical foods, devices, & diagnostics. This experience includes leadership of, and involvement in some of the most challenging and innovative products.
Cato Research has in-house capabilities to assist sponsors with all aspects of the drug development process, including the following activities:
Regulatory assessments and strategy development Interactions with regulators, including authoring and managing submissions Preclinical/toxicology development programs; study management and monitoring Pharmacokinetic study design and management Clinical strategy Phase 1 through Phase 4 clinical study design, implementation, trial management, and monitoring services Data management Statistical analyses and integrated statistical/clinical study reports Medical affairs Medical writing Program and project management Safety and pharmacovigilance Chemistry, manufacturing, and control programs Quality Clinical Trial Oversight Quality assurance, including audit and compliance activities for GCP, GLP and GMP Due diligence activities for emerging technologies.
cato Europe GmbH
Phone: +49 2234 37944-0
Fax: +49 2234 37944-25
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