Cadore provides consulting services in the field of drug development. We cover all phases of product development including pharmaceutical development, non-clinical and clinical trials as well as support during marketing authorization application submissions and assessment in the EU. We bridge the gap between basic research and clinical applications by applying rigorous scientific methods and standards to validate the drug candidates and ensure their quality and safety. We optimize preclinical studies and clinical trials in compliance with regulatory requirements and ethical principles. Our expertise covers medicinal products from simple formulations such as immediate-release oral dosage forms to new chemical entities and complex dosage forms and routes of administration such as long-acting injectibles or locally acting products in the lungs, skin or gastrointestinal system. Our experts have extensive experience in various fields of drug discovery and development, such as pharmacology, toxicology, chemistry, bioinformatics and clinical research. Together, we create for our clients the tailor-made solutions that comply with the regulatory standards and are cost-and time-effective.