The effective management of the clinical phase is paramount to the success of your medical device or digital health application. MEDIACC delivers all-encompassing support and vigilant supervision to ensure flawless study execution.
The clinical phase can present unexpected challenges and obstacles that may prove time-consuming and expensive. MEDIACC offers all necessary skills and extensive experience to ensure the smooth execution of your clinical trial, paving the way for your product's market readiness.
Prior to enrolling the first study participants (FPFV), we conduct training for the study staff during the initiation visit. We collaborate closely with clinical trial sites to ensure successful study execution.
Throughout the clinical phase, our role is to monitor the trial's progress and maintain ongoing communication with clinical trial sites. You can expect regular reports from us on trial advancement and relevant safety events (vigilance).
As soon as the last study participant has completed the study (LPLV), we check the complete study documentation. After this review, the clinical trial site or the digital trial center including the digital study platform is closed (close-out visit).
Our many years of experience in study design enable us to offer you effective and customized strategies for your products. With us at your side, you can be sure not to lose valuable time in developing a suitable project strategy.
We are proud of our numerous satisfied customers as well as our success stories of past projects. Every step of the way, we ensure that your study implementation runs efficiently and that your medical devices or digital health applications find their way to successful market approval.
With our comprehensive support and years of experience in clinical trials, you can be sure that your trial execution will be efficient and pave the way for your medical devices or digital health applications to reach the market.