Device Development Services
IDA Consultants provides a wide array of device specific development services through our team of highly experienced consultants
Development Planning
By looking at the specific needs of your technology and the regulatory and market requirements we work to plan cost effective and innovative programmes to fast track you into the market place.
Regulatory Strategy
Our in depth knowledge of the regulations we are able to help you through the maze of development, classify your device and plan the work needed to gain approval.
CE Marking
We are not a notified body but we know how to work with them to best effect ensuring your product obtains its CE mark with minimum fuss
Clinical Trial Execution
Once you know what your going to do, there are many hurdles to overcome, ethics approval and trial documentation, and vigilance systems will pull it all together and delivery your clinical trial.
Prototyping and design
we team work with the best people and facilities to get designs that work and prototypes you can use in testing, we facilitate the process with minimum fuss and expense.
Regulatory Submissions
we put your documentation together and manage your submissions, marketing approvals, CE marks in Europe and in the USA.
Get in touch for more information.
I would like to receive more information concerning services on medical devices Clinical.
Ester PVL.MD