Stridon Clinical Research LTD

stridon clinical research is a cro specialising in medical writing and regulatory affairs. we help our pharma and biotech clients get regulatory approval for their clinical trials, with no hassle and at the first attempt, by producing expertly written, high quality clinical trial and regulatory documentation. our team of medical writers and regulatory specialists are located in the uk, us and europe. their extensive medical writing experience and intimate knowledge of nuanced differences in international regulatory requirements give us unrivalled ability to author clinical trial documentation to the highest quality and scientific standards, ready for submission to regulatory authorities worldwide. we work remotely, without geographical constraints, either on our clients’ document management systems or on stridon’s secure, collaborative platform. this allows our medical writers to become an extension of your team, being responsive and flexible to your needs. all documents produced by