We have combined our recruiting strength to better serve you, and are excited to be part of Oxford Global Resources.
The unification of our business goals enables us to continue providing the high level of service that you have come to trust from our teams, with an expanded service offering for the Sciences industry.
Support and Guidance for MDR Compliance
European Medical Device Regulations (MDR)
Risk Mitigation & Management Quality Assurance
Initial gap assessment completed within two months.
A medical device manufacturer of surgical tools was beginning their MDR compliance journey. As they had limited resources and knowledge of MDR, they decided to pursue outside support. Due to Oxford Global Resources’ organized, hands-on approach and oversight of the project, the client felt more comfortable partnering with us.
Two Oxford Quality Assurance Subject Matter Experts were selected to guide the client through an initial gap assessment of all product files. The consultants thoroughly reviewed all documentation including design history files and CERs to identify gaps and areas for remediation as the client moved from MDD compliance to MDR.
The consultants completed the initial gap assessment within two months. The client was able to strategically leverage Oxford’s services in order to prevent interruptions in their new product launch that coincided with their EU MDR efforts. Due to our ability to take ownership of the project from the beginning, regular status reports, and unmatched consultant talent, the client was able to trust their initiative was being handled with the right expertise and knowledge.