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 Stridon undergo thorough scientific, editorial and quality control review. The company is set up and run as an establishment of experienced affiliates, all experts in their field, with an equitable share in the business proceeds. This setup allows us to be agile and run the business cost effectively with negligible overheads, so that we can concentrate on what we enjoy the most - delivering honest, quality service on time.