QCTR puts quality at the heart of its work in clinical research. Our in-depth understanding of all aspects of drug development and the clinical trial process allows us to offer a consistent service to the highest of standards.
We are specialists in the therapeutic areas of psychiatry, neurology and in orphan diseases and we work to the required local, national, European and US clinical research guidelines.
Our clients can gain the benefit of our expertise with a high calibre team delivering high quality services from study design through to clinical study report.
The highly experienced QCTR team have a track record in successfully conducting clinical trials. We anticipate the potential pitfalls and offer innovative solutions to ensure your trial runs smoothly and to the required timetable.
We access leading experts, proven investigators and global centres of excellence to deliver patient recruitment in the most challenging projects.
We know what a sponsor wants from a CRO and aim to give that service.
QCTR understand the importance of transparent budgeting, and accurate, honest and timely communication. QCTR give Clients the reassurance of an accurate and clearly costed proposal, based on an agreed scope, assumptions and timelines. Only if the Client changes the scope, assumptions, or timelines will this lead to a revision of the cost.
We work closely with you to ensure you have the information you need, when you need it, and with the constant assurance that your project is on time and on budget.
Our established and experienced team and our stable network of contacts allow us to provide a consistent quality of service to guarantee the success of your project.
We have an excellent track record of delivering studies to demonstrate our reliability in various disease areas, different complexities of studies and in different geographical locations. An unbeatable 100% of our clients have supplied us with repeat business.
As a small CRO you can rely on us to care about your project as if it were our own.