Implementing the complex governing principles and guidelines of the new ISO standard can be a challenge taking up time and resources. Our Clinical Trials team is at your side as a valuable partner. Our experienced medical writers are not only well acquainted with the latest developments in your specialty, but are also proficient in the practical application of ISO 24495-1.
However, our services extend way beyond medical writing. We also offer expert translations in medicine and pharmacology, back translations, adaptations, and reviews for each phase of your clinical trial. One of our strong points is on-time delivery so that your study phases can be completed efficiently and precisely. Even last-minute changes are no problem for us – we implement them quickly and reliably.
Our dedicated team will provide you with professional support that will take your projects to a new level and save you time and resources. Please contact us to find out more about how we can help you with your clinical trials.
Contact the Clinical Trials team