The requirements associated with medical device safety testing continue to increase, which has raised the bar for...
We have recently expanded our capabilities to include MRI safety evaluation of electrically active devices to our...
Dear valued clients, With the rising global concern around COVID-19, we wish to let you know that...
The European Medical Device Regulation (MDR) is a new set of regulations that will become effective May...
Compared to the Medical Device Directive (MDD) 93/42/EEC, the Medical Device Regulation (MDR) No. 2017/745 introduces a...
Understanding the classification of your medical device before CE marking is a critical step as it affects...
To maintain compliance with heightened requirements under the Medical Device Directive (i.e., recent Notified Body implementation of...
Since 2015, MED Institute has been focused on developing its partnership with medical device and biotech companies...
In medical science reporting, ghostwriting has a bad rep. Deservedly so, in many cases. Why is this...
Part 2: Considerations for designing an electronic data capture system for clinical trials with sponsors/CRO in mind....
In clinical trials, electronic data capture (EDC) systems are widely used to collect data such as patient...
In our previous blog post, we described our preliminary regulatory research study on whether our client’s electronic...
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