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Monitoring

Clinical studies are costly and time-consuming measures to evaluate the performance and safety of medical devices. Monitoring plays an essential role in this context by means of quality control of clinical study data. The focus here is whether the investigation plan is implemented in compliance with the regulatory requirements.

We support you with

  • the identification and selection of study sites
  • the initiation of study sites
  • the continuous monitoring of study sites
  • the close-out of study sites

Our internal SOPs guarantee a harmonized and structured conduct during all steps.

We already have extensive experience in various indications and, thanks to our cooperation partners, are also able to supervise large multicenter studies flexibly and properly.

In this context, we also offer a seminar about monitoring of MPG- studies (Flyer).

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