You may be experienced in all aspects of clinical trials, including design, protocol, site selection, monitoring, reporting, etc. You may have experienced the journey from idea to publication, regulatory submission, and maybe even changing healthcare and medical praxis. Or maybe this is your first time. Irrespective of which, we can help you reach your specific destination.

Considering the resources needed to conduct a clinical trial, it is critical to get it right from the start. You need to base strategic decisions for your clinical program on a thorough understanding of the surrounding landscape. The landscape encompasses not only regulatory requirements, but also the market that you want to enter. You also need to consider the target audience for your concept. Wherever you are heading, you require solid and robust data that support your concept.

At SCRO, we are passionate about what we do and we are proud of what we achieve. We want to support you in your work, getting it right from the start so your downstream activities are executed in a way that ensures regulatory compliance. We have experience in handling Phase I to IV clinical trials and non-interventional studies (NIS) in compliance with GCP and the Clinical Trials Directive. We have successfully helped clients in a wide range of therapeutic areas: cardiology, oncology, urology, CNS, endocrinology, HIV, gastroenterology, anaesthesia, and many more.