Preparing your QMS for the EU MDR

Preparing Your QMS For The EU MDR

RS Ness supports Life Science companies in QA, Regulatory Affairs, Clinical Affairs, Engineering, Validation and Project Management.

Contact us to support your MDR Transition. 

How to establish DHR

DHR is an essential requirement for Medical Device Company - RS NESS

RS NESS supports the Life Science in such field as: Quality Assurance (QA), Regulatory Affairs (RA), Clinical Affairs (CA), Engineering, Validation and Project Management (PM). We provide service to the companies at different lifecycle stages incorporating end-to-end project activities while adhering to the regulatory requirements. Knowledge, professionalism, and dedication lead our highly qualified team to your success.
If you have any questions, or if you need professional support, please contact us.