Have you started the preparations to comply with the MDR in your company? Not meeting the deadline of May 2020 is not an option. Do you have clinical data available and is the data still valid to meet the clinical evaluation process requirements? Clinical evidence of safety and performance will be inevitable for your products as there will be enhanced vigilance and market surveillance.
We cannot emphasize enough to take action.
But how can we help?
Archer Research is an expert partner to manage your clinical trial. As a full-service Contract Research Organization (CRO) we support every step of your clinical research project.
Extensive data collection strategies are most challenging in the new Regulations and have to be implemented to address the MDR requirements. Clinical data management supported by Archer Research will increase the quality of your data.
Go to Investigator-driven trials and find out how we can support.