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CRO. We provide tailor-made Clinical Monitoring and Management, Regulatory, Auditing and Training services during the set-up, maintenance and closure of clinical trials with pharmaceuticals, biotech products or medical devices.
Our core activities cover Benelux, France, Germany and UK, whilst our network is operational throughout most of Europe.
Our dedicated team highly experienced in monitoring, project management, regulatory affairs, training and auditing is well acquainted with the multicultural diversity in Europe. Each team member is fluent in at least 3 languages and highly educated in (para)medical sciences.
Whether you're a small start-up biotech or medical device company, a big pharmaceutical multinational, a small one-office CRO or one of the big six CRO's, KasaConsult is your trusted and reliable partner in Europe.