CTI regulatory and drug and device development experts bridge the gap between the conceptual stages of development all the way through to execution. This includes devising global regulatory strategies, multi-national clinical trial planning/design/execution, as well as continuing global regulatory submissions through marketing approval.
We offer an integrated approach to clinical trial planning and design that includes expertise from our diverse team of medical, regulatory, and operations experts to ensure that trials are set up for successful execution and yield data that are supportive of downstream development activities.Learn More
CTI provides a global team of experienced medical writing, regulatory, and quality assurance experts that routinely serve as an extension of our sponsors to create documents required for regulatory submissions.Learn More
CTI's international regulatory strategy experts have strong regulatory and clinical backgrounds enabling us to provide custom strategy solutions for our sponsors.Learn More